Monday, 7 May 2012

Fersamal 140mg / 5ml Syrup





1. Name Of The Medicinal Product



Fersamal 140mg/5ml Syrup


2. Qualitative And Quantitative Composition



Each 5ml of syrup contains approximately 140mg ferrous fumarate BP (45mg elemental iron).



3. Pharmaceutical Form



Syrup



4. Clinical Particulars



4.1 Therapeutic Indications



Prophylaxis and treatment of iron deficiency states.



For prophylaxis during pregnancy, a combination of iron and folic acid is usually recommended.



4.2 Posology And Method Of Administration



Adults and the elderly:



a) Iron deficiency anaemia- Fersamal syrup two 5 ml spoonfuls twice a day



b) prophylaxis- Fersamal syrup one 5 ml spoonful twice a day.



Children: Full term infants and young children-half to one 5ml spoonful twice a day.



Premature infants: 0.6ml/kg/ day to 2.4 ml/kg/day.



Method of administration: Oral



Rationale:



Taking into account the content of elemental iron and the referenced recommended daily doses of the same in deficiency states and for prophylaxis, the Fersamal dosing is in need of revision.



Each 5 mls of Fersamal syrup contains 140 mg Ferrous Fumarate which approximates to 45 mg of elemental iron – section 2 SmPC.



Recommended doses:



(a) Iron deficiency anaemia: 100 to 200 mg elemental iron per day – reference (1) BNF (2) G&G. This equates most closely to Fersamal syrup two 5 ml spoonfuls twice a day.



(b) Prophylaxis: ferrous sulphate 200 mg once or twice a day (reference BNF) i.e. 60 to 120 mg elemental iron per day. This equates most closely to Fersamal syrup one 5ml spoonful twice a day.



4.3 Contraindications



Known hypersensitivity to any of the ingredients of the product. Paroxysmal nocturnal haemoglobinuria. Haemosiderosis, haemochromatosis. Active peptic ulcer. Repeated blood transfusions. Regional enteritis and ulcerative colitis. Must not be used in anaemias other than those due to iron deficiency.



4.4 Special Warnings And Precautions For Use



Some post-gastrectomy patients show poor absorption of iron. Care is required when treating patients with iron deficiency anaemia who have treated or controlled peptic ulceration.



Duration of treatment of uncomplicated iron deficiency anaemia should not usually exceed 6 months (3 months after reversal of the anaemia has been achieved).



Because anaemia due to combined iron and Vitamin B12 or folate deficiencies may be microcytic in type, patients with microcytic anaemia resistant to treatment with iron alone should be screened for Vitamin B12 or folate deficiency.



Fersamal syrup should be kept out of the reach of children.



Long-term treatment with Fersamal syrup may increase the risk of dental caries. Adequate dental hygiene must be maintained. Since Fersamal syrup contains sugar, care must be exercised when using in patients with diabetes mellitus.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



Iron reduces the absorption of penicillamine, bisphosphonates, ciprofloxacin, entacapone, levodopa, levofloxacin, levothyroxine (thyroxine) (give at least 2 hours apart), moxifloxacin, mycophenolate, norfloxacin, ofloxacin, zinc. Absorption of both iron and antibiotic may be reduced if Fersamal 140mg/5ml is given with tetracycline. Absorption of oral iron is reduced by calcium salts, Magnesium salts (as magnesium trisilicate), Trientine.



Chloramphenicol delays plasma iron clearance, incorporation of iron into red blood cells and interferes with erythropoiesis. Some inhibition of iron absorption may occur if it is taken with cholestyramine, tea, eggs or milk.



Avoid concomitant use of iron with dimercaprol.



Oral iron antagonises hypotensive effect of methyldopa.



4.6 Pregnancy And Lactation



Administration during the first trimester of pregnancy may be undesirable.



4.7 Effects On Ability To Drive And Use Machines



None known.



4.8 Undesirable Effects



The commonest side effects relate to gastrointestinal irritation (nausea, epigastric pain, constipation or diarrhoea). In the event of these ADRs, it may be helpful to reduce the dose or switch to an alternative iron salt.



Darkening of stools, black discoloration of the teeth and allergic reactions (due to metabisulphite in the syrup vehicle) may also occur



4.9 Overdose



Acute overdosage of oral iron requires emergency treatment. In young children, 200 to 250mg/kg ferrous fumarate is considered to be extremely dangerous.



Symptoms and signs of abdominal pain, vomiting and diarrhoea occur within 60 minutes of ingestion of an overdose.



Cardiovascular collapse and coma may follow. Some spontaneous improvement may occur after this, and in some patients there is recovery. In other patients, after about 16 hours, deterioration may occur with diffuse vascular congestion, pulmonary oedema, convulsions, anuria, hypothermia, severe shock, metabolic acidosis, coagulation abnormalities, or hypoglycaemia.



Vomiting should be induced immediately, followed by parenteral injection of desferrioxamine mesylate and then gastric lavage. In the meantime, it is useful to give milk and/or 5% bicarbonate solution by mouth.



Desferrioxamine mesylate is given intramuscularly - dissolve 2 gm desferrioxamine mesylate in 2 or 3 ml of water for injection.



A solution of 5 gm desferrioxamine mesylate in 50 to 100 ml of fluid may be left in the stomach. If desferrioxamine is not available, leave 300ml of 1% to 5% sodium bicarbonate solution in the stomach. Fluid replacement is essential. Recovery may be complicated by long term sequelae, such as hepatic necrosis, pyloric stenosis, or acute toxic encephalitis which may cause CNS damage.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Iron is an essential constituent of the body, and is necessary for haemoglobin formation and for the oxidative processes of living tissues. Iron and iron salts should be given for the treatment or prophylaxis of iron deficiency anaemias. Preparations of iron are administered by mouth, by intramuscular or intravenous injection.



Soluble ferrous salts are most effective by mouth. Ferrous fumarate is an easily absorbed source of iron for replacement therapy. It is a salt of ferrous iron with an organic acid and is less irritant to the gastro-intestinal tract than salts with inorganic acids.



5.2 Pharmacokinetic Properties



In the acid conditions of the gastric contents, ferrous fumarate is dissociated and ferrous ions are liberated. These ions are absorbed in the proximal portion of the duodenum.



The ferrous iron absorbed by the mucosal cells of the duodenum is oxidised to the ferric form, and this is bound to protein to form Ferritin.



Ferritin in the mucosal cells releases iron into the blood, where it is bound to transferrin and passed into the iron stores - liver, spleen, and bone marrow.



These stores are a reserve of iron for synthesis of haemoglobin, myoglobin, and iron containing enzymes.



Iron is lost from the body through loss of cells in urine, faeces, hair, skin, sputum, nails, and mucosal cells, and through blood loss.



Ferrous fumarate has the same pattern of absorption and excretion as dietary iron.



5.3 Preclinical Safety Data



No further data.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Nipastat GL 75



Methylcellulose 20 BP



Liquid glucose BPC



Granulated sugar BP



Granular lecithin (97% A1)



Elderberry flavour (Bush C7529)



Sodium metabisulphite BP



Purified water BP



6.2 Incompatibilities



None.



6.3 Shelf Life



24 months.



6.4 Special Precautions For Storage



Protect from light. Store below 25°C.



6.5 Nature And Contents Of Container



Amber glass bottle with polypropylene cap and melinex/pulpboard/aluminium wad containing 200 ml of Fersamal 140mg/5ml syrup.



6.6 Special Precautions For Disposal And Other Handling



None.



7. Marketing Authorisation Holder



Goldshield Pharmaceuticals Limited



NLA Tower, 12-16 Addiscombe Road



Croydon, Surrey, CR0 0XT,



United Kingdom



8. Marketing Authorisation Number(S)



PL 12762/0223



9. Date Of First Authorisation/Renewal Of The Authorisation



02/12/1993



10. Date Of Revision Of The Text



29/06/2010




Sunday, 6 May 2012

Nitrolingual Duo Pack oral/sublingual


Generic Name: nitroglycerin (oral/sublingual) (NYE troe GLI ser in (OR al/sub LIN gwal))

Brand Names: Nitro-Time, Nitrolingual, Nitrolingual Duo Pack, Nitromist, Nitrostat


What is nitroglycerin?

Nitroglycerin is in a group of drugs called nitrates. Nitroglycerin dilates (widens) blood vessels, making it easier for blood to flow through them and easier for the heart to pump.


Nitroglycerin is used to treat or prevent attacks of chest pain (angina).


Nitroglycerin may also be used for purposes not listed in this medication guide.


What is the most important information I should know about nitroglycerin?


Do not use nitroglycerin if you are taking sildenafil (Viagra, Revatio), tadalafil (Cialis), or vardenafil (Levitra). Serious, life-threatening side effects can occur if you take nitroglycerin while you are using sildenafil.

Nitroglycerin can cause severe headaches, especially when you first start using it. These headaches may gradually become less severe as you continue to use nitroglycerin. Do not stop taking the medication. Ask your doctor before using any headache pain medication.


What should I discuss with my healthcare provider before taking nitroglycerin?


Do not use nitroglycerin if you are taking sildenafil (Viagra, Revatio), tadalafil (Cialis), or vardenafil (Levitra). Serious, life-threatening side effects can occur if you take nitroglycerin while you are using sildenafil.

Do not use this medication without the advice of a doctor if you have early signs of a heart attack (chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling). Seek emergency medical attention if you have symptoms of a heart attack.


You should not use this medication if you are allergic to nitroglycerin or other nitrates such as isosorbide dinitrate (Dilatrate, Isordil, Isochron) or isosorbide mononitrate (Imdur, ISMO, Monoket), or if you have:

  • severe anemia (a lack of red blood cells); or




  • a brain injury, hemorrhage, or tumor.



To make sure you can safely take nitroglycerin, tell your doctor if you have any of these other conditions:



  • congestive heart failure;




  • a history of heart attack, stroke, or head injury;




  • low blood pressure;




  • glaucoma;




  • migraine headaches; or



  • liver disease.


FDA pregnancy category C. It is not known whether nitroglycerin will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. It is not known whether nitroglycerin passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Nitroglycerin can cause severe headaches, especially when you first start using it. These headaches may gradually become less severe as you continue to use nitroglycerin. Do not stop taking the medication. Ask your doctor before using any headache pain medication.


How should I take nitroglycerin?


Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.


If possible, try to rest or stay seated when you use this medication. Nitroglycerin can cause dizziness or fainting.


If you use nitroglycerin sublingual spray to treat an angina attack: At the first sign of an attack, apply the spray directly on or under your tongue. Close your mouth after each spray. Do not inhale the spray. Do not shake the spray before or during use. You may use additional sprays every 5 minutes, but not more than 3 sprays in 15 minutes.


You may use nitroglycerin spray within 5 to 10 minutes before an activity you think might cause chest pain. Follow your doctor's instructions.


The nitroglycerin sublingual tablet should be placed under your tongue and allowed to dissolve slowly. Do not chew or swallow it. You may use additional tablets every 5 minutes, but not more than 3 tablets in 15 minutes.


Seek emergency medical attention if your chest pain gets worse or lasts more than 5 minutes, especially if you have trouble breathing or feel weak, dizzy, or nauseated, or lightheaded. You may feel a slight burning or stinging in your mouth when you use this medication. However, this sensation is not a sign of how well the medication is working. Do not use more medication just because you do not feel a burning or stinging. Do not crush, chew, break, or open an extended-release capsule. Swallow the pill whole. It is specially made to release medicine slowly in the body. Breaking or opening the pill would cause too much of the drug to be released at one time.

This medication can cause unusual results with certain medical tests. Tell any doctor who treats you that you are using nitroglycerin.


Keep this medicine on hand at all times in case of an angina attack. Get your prescription refilled before you run out of medicine completely.


If you take nitroglycerin on a regular schedule to prevent angina, do not stop taking it suddenly or you could have a severe attack of angina. Store the tablets in the glass container at room temperature, away from moisture and heat. Keep the spray away from open flame or high heat, such as in a car on a hot day. The canister may explode if it gets too hot.

What happens if I miss a dose?


Since nitroglycerin is taken as needed, you may not be on a dosing schedule. If you are taking the medication regularly, take the missed dose as soon as you remember. Skip the missed dose if your next dose is less than 2 hours away. Do not take extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of nitroglycerin can be fatal.

Overdose symptoms may include a severe throbbing headache, confusion, fever, fast or pounding heartbeats, dizziness, vision problems, nausea, vomiting, bloody diarrhea, trouble breathing, cold or clammy skin, feeling light-headed, fainting, and seizures.


What should I avoid while taking nitroglycerin?


Nitroglycerin can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol. It can increase some of the side effects of nitroglycerin, such as dizziness, drowsiness, feeling light-headed, or fainting.

Nitroglycerin side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have a serious side effect such as:

  • fast, slow, pounding, or uneven heart rate;




  • blurred vision or dry mouth;




  • nausea, vomiting, sweating, pale skin, feeling like you might pass out; or




  • fever, sore throat, and headache with a severe blistering, peeling, and red skin rash.



Less serious side effects may include:



  • mild burning or tingling with the tablet in your mouth;




  • warmth, redness, or tingly feeling under your skin; or




  • feeling weak or dizzy.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect nitroglycerin?


Many drugs can interact with nitroglycerin. Below is just a partial list. Tell your doctor if you are using:



  • alteplase (Activase);




  • aspirin or heparin;




  • bladder or urinary medications such as oxybutynin (Ditropan) or tolterodine (Detrol);




  • blood pressure medication;




  • bronchodilators such as ipratropium (Atrovent) or tiotropium (Spiriva);




  • dihydroergotamine (D.H.E. 45, Migranal) or ergotamine (Ergomar, Cafergot, and others);




  • an antidepressant such as amitriptyline (Elavil, Vanatrip, Limbitrol), clomipramine (Anafranil), imipramine (Tofranil), and others;




  • a beta-blocker such as atenolol (Tenormin), carvedilol (Coreg), metoprolol (Lopressor, Toprol), nadolol (Corgard), propranolol (Inderal), sotalol (Betapace), and others;




  • a calcium channel blocker such as diltiazem (Tiazac, Cardizem), nifedipine (Procardia), nimodipine (Nimotop), verapamil (Calan, Covera, Verelan), and others;




  • irritable bowel medications such as dicyclomine (Bentyl), hyoscyamine (Anaspaz, Cystospaz, and others), or propantheline (Pro-Banthine);




  • any medication that causes dry mouth; or




  • medicines to treat psychiatric disorders, such as chlorpromazine (Thorazine), haloperidol (Haldol), thioridazine (Mellaril), and others.



This list is not complete and there are many other drugs that can interact with nitroglycerin. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More Nitrolingual Duo Pack resources


  • Nitrolingual Duo Pack Side Effects (in more detail)
  • Nitrolingual Duo Pack Use in Pregnancy & Breastfeeding
  • Nitrolingual Duo Pack Drug Interactions
  • Nitrolingual Duo Pack Support Group
  • 3 Reviews for Nitrolingual Duo Pack - Add your own review/rating


Compare Nitrolingual Duo Pack with other medications


  • Angina
  • Angina Pectoris Prophylaxis
  • Heart Attack
  • Heart Failure
  • High Blood Pressure


Where can I get more information?


  • Your pharmacist can provide more information about nitroglycerin.

See also: Nitrolingual Duo Pack side effects (in more detail)


Saturday, 5 May 2012

Penbutolol


Pronunciation: pen-BUE-toe-lol
Generic Name: Penbutolol
Brand Name: Levatol

Do not suddenly stop taking Penbutolol. Sharp chest pain, irregular heartbeat, and sometimes heart attack may occur if you suddenly stop Penbutolol. The risk may be greater if you have certain types of heart disease. Your doctor should slowly lower your dose over several weeks if you need to stop taking it. This should be done even if you only take Penbutolol for high blood pressure. Heart disease is common and you may not know you have it. Limit physical activity while you are lowering your dose. If new or worsened chest pain or other heart problems occur, contact your doctor right away. You may need to start taking Penbutolol again.





Penbutolol is used for:

Treating mild to moderate high blood pressure. It may be used alone or with other medicines. It may also be used for other conditions as determined by your doctor.


Penbutolol is a beta-blocker. It works by slowing down the heart and decreasing the amount of blood it pumps out. This decreases blood pressure, helps the heart pump more efficiently, and reduces the workload on the heart.


Do NOT use Penbutolol if:


  • you are allergic to any ingredient in Penbutolol

  • you have a very slow heartbeat, heart block, uncontrolled heart failure, or shock caused by severe heart problems

  • you have asthma

  • you are currently taking mibefradil

Contact your doctor or health care provider right away if any of these apply to you.



Before using Penbutolol:


Some medical conditions may interact with Penbutolol. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have or have ever had an adrenal gland tumor (pheochromocytoma); lung or breathing problems (eg, asthma, chronic bronchitis, chronic obstructive pulmonary disease [COPD], emphysema); blood vessel problems; diabetes; kidney problems; low blood sugar; or an overactive thyroid

  • if you have low blood pressure or a history of heart problems (eg, heart attack, slow or irregular heartbeat, heart failure, chest pain or angina), blood circulation problems, or liver problems

  • if you will be having surgery

Some MEDICINES MAY INTERACT with Penbutolol. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Antiarrhythmics (eg, flecainide), calcium channel blockers (eg, nifedipine, diltiazem, verapamil), catecholamine-depleting agents (eg, reserpine), digoxin, diuretics (eg, furosemide, hydrochlorothiazide), fingolimod, mefloquine, mibefradil, or vasodilators (eg, hydralazine) because the risk of certain side effects may be increased (eg, very slow heart rate, very low blood pressure, fainting, severe dizziness, light-headedness)

  • Clonidine because stopping either it or Penbutolol suddenly can lead to a severe increase in blood pressure

  • Barbiturates (eg, phenobarbital) or indomethacin because they may decrease Penbutolol's effectiveness

  • Alfuzosin, insulin, nateglinide, prazosin, or repaglinide because the risk of their side effects may be increased by Penbutolol

  • Sympathomimetics (eg, albuterol) or theophyllines (eg, aminophylline) because their effectiveness may be decreased by Penbutolol

  • Epinephrine because its effectiveness may be decreased and the risk of its side effects may be increased

This may not be a complete list of all interactions that may occur. Ask your health care provider if Penbutolol may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Penbutolol:


Use Penbutolol as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Penbutolol may be taken with or without food.

  • Take Penbutolol at the same time each day.

  • Continue to use Penbutolol even if you feel well. Do not miss any doses.

  • If you miss a dose of Penbutolol, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Penbutolol.



Important safety information:


  • Penbutolol may cause dizziness or light-headedness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Penbutolol. Using Penbutolol alone, with certain other medicines, or with alcohol may lessen your ability to drive or to perform other potentially dangerous tasks.

  • Penbutolol may cause dizziness, light-headedness, or fainting. Alcohol, hot weather, exercise, and fever can increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Also, sit or lie down at the first sign of dizziness, light-headedness, or weakness.

  • Do not suddenly stop taking Penbutolol without first checking with your doctor. If your doctor decides you should no longer use Penbutolol, you will need to stop Penbutolol gradually according to your doctor's instructions.

  • It may take up to 2 weeks or longer for Penbutolol to fully work. Do not change your dose without checking with your doctor.

  • Patients being treated for high blood pressure often feel tired or run down for a few weeks after beginning therapy. Continue taking your medication even though you may not feel quite "normal." Contact your doctor or pharmacist about any new symptoms.

  • Penbutolol may mask certain signs of overactive thyroid (eg, fast heartbeat). If you have or may have overactive thyroid, do not suddenly stop taking Penbutolol. Suddenly stopping Penbutolol could worsen your condition. Discuss any questions or concerns with your doctor.

  • If you have a history of any severe allergic reaction, talk with your doctor. You may be at risk of an even more severe allergic reaction if you come into contact with the substance that caused your allergy. Some medicines used to treat severe allergies may also not work as well while you are using Penbutolol.

  • If your doctor has instructed you to check your blood pressure and heart rate regularly, be sure to do so.

  • Do not take any medicines used for colds, congestion, or weight loss without first talking with your doctor or pharmacist.

  • Diabetes patients - Penbutolol may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

  • Diabetes patients - Penbutolol may mask signs of low blood sugar, such as a rapid heartbeat. Be sure to watch for other signs of low blood sugar. Low blood sugar may make you anxious, sweaty, weak, dizzy, drowsy, or faint. It may also make your vision change; give you a headache, chills, or tremors; or make you more hungry. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

  • Before having any surgical or dental procedures or receiving emergency treatment, tell the doctor or dentist in charge that you are receiving Penbutolol.

  • Penbutolol may interfere with certain lab tests, including the glaucoma screening test. Be sure your doctor and lab personnel know you are taking Penbutolol.

  • Lab tests may be performed to monitor your progress or to check for side effects. Be sure to keep all doctor and lab appointments.

  • Use Penbutolol with caution in the ELDERLY because they may be more sensitive to its effects, especially slow heartbeat.

  • Use Penbutolol with extreme caution in CHILDREN. Safety and effectiveness have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: If you plan on becoming pregnant, discuss with your doctor the benefits and risks of using Penbutolol during pregnancy. It is unknown if Penbutolol is excreted in breast milk. If you are or will be breast-feeding while you are using Penbutolol, check with your doctor or pharmacist to discuss the risks to your baby.

If you suddenly stop taking Penbutolol, you may experience WITHDRAWAL symptoms, including worsening chest pain along with possible heart attack.



Possible side effects of Penbutolol:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Diarrhea; dizziness; headache; indigestion; light-headedness; nausea; tiredness; weakness.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; fainting; fever with aching and sore throat; mental or mood changes (eg, confusion, depression, short-term memory loss); severe or persistent dizziness; severe or persistent stomach pain; shortness of breath; slow or irregular heartbeat; sudden, unexplained weight gain; swelling of the hands, ankles, or feet; unusual bruising or bleeding; wheezing.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Penbutolol side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include difficulty breathing; fainting; severe dizziness or light-headedness; shortness of breath; slow or irregular heartbeat; swelling of the hands, ankles, or feet; wheezing.


Proper storage of Penbutolol:

Store Penbutolol at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Penbutolol out of the reach of children and away from pets.


General information:


  • If you have any questions about Penbutolol, please talk with your doctor, pharmacist, or other health care provider.

  • Penbutolol is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Penbutolol. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Penbutolol resources


  • Penbutolol Side Effects (in more detail)
  • Penbutolol Use in Pregnancy & Breastfeeding
  • Penbutolol Drug Interactions
  • Penbutolol Support Group
  • 0 Reviews for Penbutolol - Add your own review/rating


  • penbutolol Advanced Consumer (Micromedex) - Includes Dosage Information

  • penbutolol Concise Consumer Information (Cerner Multum)

  • Levatol Prescribing Information (FDA)



Compare Penbutolol with other medications


  • Angina Pectoris Prophylaxis
  • High Blood Pressure

Thursday, 3 May 2012

Iveegam


Generic Name: immune globulin (Intramuscular route, Intravenous route, Subcutaneous route)


i-MUNE GLOB-ue-lin


Intravenous route(Powder for Solution;Solution)

Immune globulin intravenous (IGIV) products have been reported to be associated with renal dysfunction, acute renal failure, osmotic nephrosis, and death. Use caution in patients predisposed to acute renal failure and administer at the minimum concentration available and the minimum rate of infusion practicable in such patients. Higher rates of renal failure were associated with IGIV products containing sucrose . Flebogamma(R) 5%, Flebogamma(R) 5% DIF, Flebogamma(R) 10% DIF, Gammagard (R), Gamunex(R)-C, and Previgen(R) do not contain sucrose . Glycine is used as a stabilizer in Gamunex(R)-C .


Subcutaneous route(Solution)

Immune globulin intravenous (IGIV) products have been reported to be associated with renal dysfunction, acute renal failure, osmotic nephrosis, and death. Use caution in patients predisposed to acute renal failure and administer at the minimum concentration available and the minimum rate of infusion practicable in such patients. Higher rates of renal failure were associated with IGIV products containing sucrose. Gammagard(R) does not contain sucrose .



Commonly used brand name(s)

In the U.S.


  • Baygam

  • Carimune

  • Gamimune N

  • Gammagard

  • Gammar-P

  • Hizentra

  • Iveegam EN

  • Octagam

  • Panglobulin NF

  • Polygam S/D

  • Sandoglobulin

  • Vivaglobin

Available Dosage Forms:


  • Solution

  • Powder for Solution

Therapeutic Class: Immune Serum


Uses For Iveegam


Immune globulin injection belongs to a group of medicines known as immunizing agents. It is used to prevent or treat diseases that occur when your body has a weak immune system. Immune globulin contains antibodies that make your immune system stronger. It is used for patients who have primary humoral immunodeficiency (PI), idiopathic thrombocytopenic purpura (ITP), and chronic inflammatory demyelinating polyneuropathy (CIDP).


This medicine is to be administered only by or under the supervision of your doctor.


Once a medicine has been approved for marketing for a certain use, experience may show that it is also useful for other medical problems. Although these uses are not included in product labeling, immune globulin is used in certain patients with the following medical conditions:


  • Chronic parvovirus B19 infection (treatment).

  • Dermatomyositis (treatment).

  • Guillain-Barré syndrome (treatment).

  • Hyperimmunoglobulinemia E syndrome (treatment).

  • Infections in low-birth-weight preterm high-risk neonates (prophylaxis and treatment adjunct).

  • Lambert-Eaton myasthenic syndrome (treatment).

  • Multifocal motor neuropathy (treatment).

  • Relapsing-remitting multiple sclerosis (treatment).

Before Using Iveegam


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of immune globulin injection in children. However, safety and efficacy have not been established in children with CIDP, safety and efficacy have not been established for Flebogamma® and subcutaneous injection of Gamunex®-C in children with PI, and safety and efficacy have not been established for Gammagard Liquid and Vivaglobin® in children younger than 2 years of age.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of immune globulin injection in the elderly. However, elderly patients are more likely to have age-related blood clotting problems, kidney disease, or heart disease, which may require caution for patients receiving immune globulin injection.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

Breast Feeding


Studies in women suggest that this medication poses minimal risk to the infant when used during breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.


Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Anemia, history of or

  • Bleeding problems, history of or

  • Hyponatremia (low sodium in the blood) or

  • Kidney problems—Use with caution. May make these conditions worse.

  • Atherosclerosis (hardening of the arteries), history of or

  • Blood clotting problems, history of or

  • Diabetes or

  • Heart attack or stroke, recent or

  • Heart or blood vessel disease or

  • Hyperproteinemia (high protein in the blood) or

  • Hyperviscosity (thick blood), known or suspected or

  • Hypovolemia (low blood volume or major loss of body fluids) or

  • IgA (immunoglobulin A) deficiency with antibodies against IgA or

  • Paraproteinemia (paraproteins in the blood) or

  • Sepsis (serious infection in the body)—Use with caution. May cause side effects to become worse.

Proper Use of immune globulin

This section provides information on the proper use of a number of products that contain immune globulin. It may not be specific to Iveegam. Please read with care.


A doctor or other trained health professional will give you or your child this medicine. This medicine is given through a needle placed in one of your veins, as a shot into one of your muscles, or as a shot under your skin.


This medicine comes with a patient information insert. Read and follow the instructions carefully. Ask your doctor if you have any questions.


While you or your child are being treated with immune globulin injection, do not have any immunizations (vaccines) without your doctor's approval. Live virus vaccines should not be given for 3 months after receiving immune globulin.


The Gammagard Liquid, Gamunex®-C, Hizentra®, and Vivaglobin® products may sometimes be given at home to patients who do not need to be in the hospital or clinic. They are given as an infusion under your skin once every week. If you or your child are using this medicine at home, your doctor will teach you how to prepare and infuse the medicine. Be sure you understand how to use the medicine.


Do not change the brand or type of your immune globulin unless your doctor tells you to. If you or your child must change the brand or type of medicine, talk to your doctor before giving yourself an injection.


If you or your child are using Gammagard Liquid, Gamunex®-C, Hizentra®, or Vivaglobin® at home, you will be shown the body areas where the medicine can be given. Use a different body area each time you give yourself an infusion. Keep track of where you give each infusion to make sure you rotate body areas. This will help prevent skin problems.


Allow the Gammagard Liquid, Gamunex®-C, or Vivaglobin® brand to reach room temperature before using it.


To use Gammagard Liquid, Gamunex®-C, Hizentra®, or Vivaglobin®:


  • First, gather the items you will need on a clean, flat surface using a cloth or towel in a well-lighted area.

  • Wash your hands with soap and water before and after using this medicine.

  • If you have been told to wear gloves when preparing your infusion, put the gloves on.

  • Check the liquid in the vial (glass container). It should be clear and slightly yellow to light brown in color. If it is cloudy, discolored, or contains large flecks (particles), do not use the vial. Select another vial.

  • If the liquid is clear, place it on the clean, flat surface. Do not heat up or shake the medicine.

  • Follow your doctor's instructions on how to prepare the correct amount of medicine.

  • Choose an injection site on your body (e.g., abdomen or stomach area, thigh, upper arm, upper leg, or hip). Clean the injection site with a fresh alcohol wipe, and let it dry.

  • With two fingers, pinch together the skin at the injection site. Insert the needle with the tube under the skin.

  • Put sterile gauze and tape over the injection site to keep the needle from coming out.

  • Before starting the infusion, make sure no blood is flowing into the infusion tube. If blood is present, remove and throw away the used needle and tube.

  • Follow your doctor's instructions on how to use the infusion pump.

  • Remove the peel-off portion of the label from the used vial. Place this label in your treatment diary or log book. Write down the amount of medicine you used, the date, and the time of your treatment.

  • It usually takes about 60 minutes for each infusion.

  • When all of the medicine has been infused, turn off the pump.

  • Take the gauze off and remove the needle and tube from your skin.

  • Clean and store the infusion pump.

  • Throw away used needles and tubes in a hard, closed container that the needles cannot poke through. Keep this container away from children and pets.

Missed Dose


This medicine needs to be given on a fixed schedule. If you miss a dose or forget to use your medicine, call your doctor or pharmacist for instructions.


Storage


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Store the Hizentra® product at room temperature, away from heat and moisture. Keep from freezing.


Protect the Hizentra® product from direct light. Keep the medicine in the original package until you are ready to use it.


Store the Gamunex®-C and Vivaglobin® products in the refrigerator, but do not freeze the medicine. Store it in the original container.


You may store the Gammagard Liquid product in the refrigerator for 36 months, or at room temperature for up to 12 months (if within the first 24 months of the date of manufacture). Check the box for the date of manufacture. Store it in the original container. Do not freeze. Talk with your pharmacist if you have questions about storage of this product.


Precautions While Using Iveegam


It is very important that your doctor check the progress of you or your child at regular visits for any problems that may be caused by this medicine. Blood and urine tests may be needed to check for unwanted effects.


Patients with idiopathic thrombocytopenic purpura (ITP) should not be treated with Gamunex®-C that is injected under the skin (subcutaneously). Doing so may increase the risk of having a hematoma (buildup of blood under the skin).


This medicine may cause fever, chills, flushing, headaches, nausea, and vomiting, especially if you are receiving it for the first time or if you have not received it for more than 8 weeks. Check with your doctor or nurse right away if you have any of these symptoms.


This medicine is made from donated human blood. Some human blood products have transmitted certain viruses to people who have received them. The risk of getting a virus from medicines made from human blood has been greatly reduced in recent years. This is the result of required testing of human donors for certain viruses, and required testing of the medicine when it is made. Although the risk is low, talk with your doctor if you have concerns.


This medicine may cause a serious type of allergic reaction, including anaphylaxis, which can be life-threatening and requires immediate medical attention. Tell your doctor right away if you or your child have a rash, itching, hives, chest pain, dizziness or lightheadedness, trouble breathing, trouble swallowing, or any swelling of your hands, face, or mouth after receiving this medicine. Certain people, including those with IgA (an immunoglobulin) deficiency and antibodies against IgA and a history of hypersensitivity to human immunoglobulin products should not use this medicine.


Check with your doctor right away if you or your child start to have a stiff neck, drowsiness, fever, severe headache, nausea or vomiting, painful eye movements, or eye sensitivity to light. These could be symptoms of a serious condition called aseptic meningitis syndrome (AMS).


This medicine may cause bleeding (hemolysis) or hemolytic anemia. Tell your doctor right away if you or your child have stomach or back pain, dark urine, decreased urination, difficulty with breathing, an increased heart rate, tiredness, or yellow eyes or skin after you receive the medicine.


Check with your doctor right away if you or your child start having chest pain; difficult, fast, or noisy breathing, sometimes with wheezing; blue lips and fingernails; fever; pale skin; increased sweating; coughing that sometimes produces a pink frothy sputum; shortness of breath; or swelling of the legs and ankles, after receiving this medicine. These may be symptoms of a serious lung problem.


This medicine may cause blood clots. This is more likely to occur if you have a history of blood clotting problems, heart disease, or atherosclerosis (hardening of the arteries), or if you are obese, take medicines containing estrogen, or must stay in bed for a long time because of surgery or illness. Check with your doctor right away if you or your child suddenly have chest pain, shortness of breath, a severe headache, leg pain, or problems with vision, speech, or walking. .


Check with your doctor right away if you or your child start having red or dark brown urine; lower back or side pain; a sudden weight gain; a swollen face, arms, or legs; decreased urine output; or any problems with urination after you receive this medicine. These may be symptoms of a serious kidney problem.


Make sure any doctor or dentist who treats you knows that you are using this medicine. This medicine may affect the results of certain medical tests.


Iveegam Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor or nurse immediately if any of the following side effects occur:


More common
  • Chills

  • cough

  • difficulty with breathing

  • fast, pounding, or irregular heartbeat or pulse

  • fever

  • noisy breathing

  • shortness of breath

  • tightness in the chest

  • troubled breathing

  • unusual tiredness or weakness

Less common
  • Bluish coloring of the lips or nailbeds

  • burning sensation in the head

  • faintness or lightheadedness

Rare
  • Difficulty with swallowing

  • hives or welts

  • itching, especially of the feet or hands

  • reddening of the skin, especially around the ears

  • swelling of the eyes, face, or inside of the nose

Incidence not known
  • Back, leg, or stomach pains

  • bleeding gums

  • blistering, peeling, or loosening of the skin

  • bloody, black, or tarry stools

  • blurred vision

  • change in consciousness

  • chest pain or discomfort

  • cold, clammy, or pale skin

  • confusion

  • convulsions

  • coughing that sometimes produces a pink frothy sputum

  • dark urine

  • decrease in urine amount

  • dizziness, faintness, or lightheadedness when getting up suddenly from a lying or sitting position

  • fever with or without chills

  • headache that is severe and occurs suddenly

  • increased sweating

  • light-colored stools

  • loss of appetite

  • loss of bladder control

  • loss of consciousness

  • low blood pressure or pulse

  • muscle spasm or jerking of all extremities

  • nausea or vomiting

  • nosebleeds

  • painful or difficult urination

  • pains in the chest, groin, or legs, especially calves of the legs

  • red skin lesions, often with a purple center

  • red, irritated eyes

  • shakiness in the legs, arms, hands, or feet

  • shivering

  • skin blisters

  • slurred speech that occurs suddenly

  • slow breathing

  • sores, ulcers, or white spots in the mouth or on the lips

  • sudden loss of consciousness

  • sudden loss of coordination

  • sudden vision changes

  • sudden, severe weakness or numbness in the arm or leg

  • sweating

  • swelling in the legs and ankles

  • tightness in the chest

  • trembling or shaking of the hands or feet

  • unusual bleeding or bruising

  • yellow eyes or skin

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


More common
  • Diarrhea

  • dizziness

  • headache

  • joint pain

  • muscle pain

  • redness, swelling, itching, or pain at the injection site

  • skin rash

Less common
  • Hip pain

  • leg cramps

Incidence not known
  • Feeling of warmth

  • redness of the face, neck, arms, and occasionally, upper chest

  • stomach pain

  • swollen glands

  • tiredness

  • weakness

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.


More Iveegam resources


  • Iveegam Use in Pregnancy & Breastfeeding
  • Iveegam Drug Interactions
  • Iveegam Support Group
  • 5 Reviews for Iveegam - Add your own review/rating


  • Carimune Prescribing Information (FDA)

  • Flebogamma MedFacts Consumer Leaflet (Wolters Kluwer)

  • Flebogamma Prescribing Information (FDA)

  • Gammaplex Prescribing Information (FDA)

  • Gammar-P I.V. Consumer Overview

  • Gammar-P I.V.

  • Gamunex MedFacts Consumer Leaflet (Wolters Kluwer)

  • Gamunex Consumer Overview

  • Octagam Prescribing Information (FDA)

  • Octagam Consumer Overview

  • Privigen Prescribing Information (FDA)

  • Privigen Consumer Overview



Compare Iveegam with other medications


  • Autoimmune Neutropenia
  • Bone Marrow Transplantation
  • Chronic Inflammatory Demyelinating Polyradiculoneuropathy
  • Chronic Lymphocytic Leukemia
  • Evan's Syndrome
  • HIV Infection
  • Idiopathic Thrombocytopenic Purpura
  • Kawasaki Disease
  • Myasthenia Gravis
  • Polymyositis/Dermatomyositis
  • Primary Immunodeficiency Syndrome

UR N-C


Generic Name: hyoscyamine, methenamine, methylene blue, phenyl salicylate, and sodium phosphate (Oral route)


hye-oh-SYE-a-meen SUL-fate, meth-EN-a-meen, METH-i-leen BLOO, FEN-il sal-I-si-late, SOE-dee-um FOS-fate, mono-BAY-sik


Commonly used brand name(s)

In the U.S.


  • Phosphasal

  • Urelle

  • Uretron D/S

  • Uribel

  • Urimar-T

  • UR N-C

  • Ustell

  • Uticap

  • Utira-C

  • Utrona-C

Available Dosage Forms:


  • Tablet

  • Capsule

  • Tablet, Enteric Coated

  • Tablet, Extended Release

Therapeutic Class: Urinary Antispasmodic


Pharmacologic Class: Hyoscyamine


Chemical Class: Salicylate, Non-Aspirin


Uses For UR N-C


Urelle® is a combination of five medicines: hyoscyamine, methenamine, methylene blue, phenyl salicylate, and sodium phosphate. It is used to relieve discomfort, swelling, pain, frequent urge to urinate, and cramps or spasms of the urinary tract caused by an infection or a diagnostic procedure.


Hyoscyamine is an antispasmodic drug, which relieves muscle cramps or spasms. Methenamine and methylene blue are antiseptic drugs, which help clear a urinary tract infection. Phenyl salicylate is a pain reliever. Sodium phosphate makes the urine more acidic, which helps methenamine work better.


This medicine is available only with your doctor's prescription.


Before Using UR N-C


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of Urelle® in children. However, use is not recommended in children 6 years of age and younger.


Geriatric


No information is available on the relationship of age to the effects of Urelle® in geriatric patients.


Breast Feeding


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.


  • Amitriptyline

  • Amoxapine

  • Bupropion

  • Cisapride

  • Citalopram

  • Clomipramine

  • Desipramine

  • Desvenlafaxine

  • Doxepin

  • Duloxetine

  • Escitalopram

  • Fluoxetine

  • Fluvoxamine

  • Imipramine

  • Isocarboxazid

  • Linezolid

  • Maprotiline

  • Mesoridazine

  • Mirtazapine

  • Nortriptyline

  • Paroxetine

  • Phenelzine

  • Pimozide

  • Potassium

  • Protriptyline

  • Selegiline

  • Sertraline

  • Sparfloxacin

  • Thioridazine

  • Tranylcypromine

  • Trimipramine

  • Venlafaxine

  • Vilazodone

Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Alfuzosin

  • Amiodarone

  • Amitriptyline

  • Amoxapine

  • Apomorphine

  • Arsenic Trioxide

  • Asenapine

  • Astemizole

  • Azithromycin

  • Buspirone

  • Chloroquine

  • Chlorpromazine

  • Ciprofloxacin

  • Citalopram

  • Clarithromycin

  • Clomipramine

  • Clozapine

  • Crizotinib

  • Dasatinib

  • Desipramine

  • Disopyramide

  • Dofetilide

  • Dolasetron

  • Droperidol

  • Erythromycin

  • Flecainide

  • Fluconazole

  • Gatifloxacin

  • Gemifloxacin

  • Granisetron

  • Halofantrine

  • Haloperidol

  • Ibutilide

  • Iloperidone

  • Imipramine

  • Lapatinib

  • Levofloxacin

  • Lopinavir

  • Lumefantrine

  • Mefloquine

  • Methadone

  • Moxifloxacin

  • Nefazodone

  • Nilotinib

  • Norfloxacin

  • Nortriptyline

  • Octreotide

  • Ofloxacin

  • Ondansetron

  • Paliperidone

  • Pazopanib

  • Perflutren Lipid Microsphere

  • Posaconazole

  • Procainamide

  • Prochlorperazine

  • Promethazine

  • Propafenone

  • Protriptyline

  • Quetiapine

  • Quinidine

  • Quinine

  • Ranolazine

  • Salmeterol

  • Saquinavir

  • Solifenacin

  • Sorafenib

  • Sotalol

  • Sunitinib

  • Telavancin

  • Telithromycin

  • Terfenadine

  • Tetrabenazine

  • Trazodone

  • Trimipramine

  • Vandetanib

  • Vardenafil

  • Vemurafenib

  • Voriconazole

  • Ziprasidone

Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Aluminum Carbonate, Basic

  • Aluminum Hydroxide

  • Aluminum Phosphate

  • Calcium Acetate

  • Calcium Carbonate

  • Calcium Citrate

  • Dihydroxyaluminum Aminoacetate

  • Dihydroxyaluminum Sodium Carbonate

  • Magaldrate

  • Magnesium Carbonate

  • Magnesium Hydroxide

  • Magnesium Oxide

  • Magnesium Trisilicate

Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Other Medical Problems


The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Congestive heart failure or

  • Coronary heart disease or

  • Glaucoma or

  • Heart disease (e.g., mitral stenosis) or

  • Heart rhythm problems (e.g., arrhythmia) or

  • Myasthenia gravis (severe muscle weakness) or

  • Stomach or intestinal (bowel) blockage or

  • Stomach ulcers or

  • Urinary problems (e.g., bladder blockage due to an enlarged prostate)—Use with caution. May make these conditions worse.

  • Allergy or intolerance to belladonna or salicylates—Use with caution. May be sensitive to this medicine also.

Proper Use of hyoscyamine, methenamine, methylene blue, phenyl salicylate, and sodium phosphate

This section provides information on the proper use of a number of products that contain hyoscyamine, methenamine, methylene blue, phenyl salicylate, and sodium phosphate. It may not be specific to UR N-C. Please read with care.


Take this medicine for the full time of treatment, even if you begin to feel better. Also, keep your appointments with your doctor for check-ups so that your doctor will be better able to tell you when to stop taking this medicine.


Drink extra fluids after you take this medicine so you will pass more urine.


Dosing


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For oral dosage form (tablets):
    • For treatment of symptoms of urinary tract infection or diagnostic procedure:
      • Adults—One tablet four times a day

      • Children 7 years of age and older—Use and dose must be determined by your doctor.

      • Children 6 years of age and younger—Use is not recommended.



Missed Dose


If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Precautions While Using UR N-C


It is very important that your doctor check the progress of you or your child at regular visits. This will allow your doctor to see if the medicine is working properly and to decide if you should continue to take it.


If your or your child's symptoms do not improve or if they get worse, call your doctor.


Stop using this medicine and check with your doctor right away if you or your child have blurred vision, dizziness, or rapid pulse.


This medicine will make your urine to be colored blue. This is normal and is nothing to worry about.


This medicine will not cure a serious urinary tract infection and will only work to relieve symptoms as long as you continue to take it.


Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements.


UR N-C Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor immediately if any of the following side effects occur:


Incidence not known
  • Blurred vision

  • dizziness

  • rapid pulse

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


Incidence not known
  • Blue-colored urine

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.

Sodium Chloride 0.9% w / v Solution for Injection





1. Name Of The Medicinal Product



Sodium Chloride 0.9% w/v Solution for Injection


2. Qualitative And Quantitative Composition



Each 1ml of solution contains 0.9% w/v of Sodium Chloride B.P.



3. Pharmaceutical Form



Clear, colourless, sterile solution intended for parenteral administration to human beings.



4. Clinical Particulars



4.1 Therapeutic Indications



1) For use in prophylactic and replacement therapy requiring the use of isotonic saline solution.



2) In the reconstitution, dilution and making up of certain drugs.



3) As a saline irrigant.



4) As a priming fluid for haemodialysis procedures and to initiate and terminate blood transfusions.



4.2 Posology And Method Of Administration



Route of administration: For intravenous administration, or as appropriate to the reconstituted drug.



In prophylaxis or replacement therapy of extracellular fluid deficits, the dosage of Sodium Chloride 0.9% w/v Solution for Injection is dependent on the age, weight, clinical status and degree of deficiency, and must be determined on an individual basis.



4.3 Contraindications



There are no absolute contra-indications to the use of Sodium Chloride 0.9% w/v Solution for Injection.



4.4 Special Warnings And Precautions For Use



Sodium Chloride 0.9%w/v Solution for Injection should be administered with caution to patients with congestive cardiac failure, pre-eclampsia hypertension, peripheral and pulmonary oedema and impaired renal function.



Care is also required when administering this solution to very young or to the elderly patients.



Pseudohyponatraemia is a condition in which spuriously low concentrations of sodium are found when plasma sodium is measured by conventional methods. It may occur when there is an abnormally high concentration of large molecules and hence an abnormally low percentage of plasma water. This may occur in hyperlipaemia and hyperproteinaemia and has also been reported in patients with diabetes mellitus. Correct values may be obtained by referring the concentration to plasma water.



Before use, ensure that the container is undamaged and the contents clear in appearance. After use, discard any remaining solution.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



Concomitant administration of other sodium salts may contribute to the sodium load.



Only use as a pharmaceutical diluent where indicated in the manufacturer's literature.



4.6 Pregnancy And Lactation



The solution is physiological saline and may be used during pregnancy and lactation.



4.7 Effects On Ability To Drive And Use Machines



None



4.8 Undesirable Effects



Injudicious intravenous saline therapy (e.g. post-operatively and in patients with impaired cardiac or renal function) may cause hypernatraemia. Osmotically induced water shifts decrease intracellular volume, resulting in dehydration of internal organs, especially the brain, which may lead to thrombosis and haemorrhage.



General adverse effects of sodium chloride excess in the body include nausea, vomiting, diarrhoea, abdominal cramps, thirst, reduced salivary and lachrymal secretions, sweating, fever, hypotension, tachycardia, renal failure, peripheral and pulmonary oedema, respiratory arrest, headache, dizziness, restlessness, irritability, weakness, muscular twitching and rigidity, convulsions, coma and death. Excess chloride in the body may cause a loss of bicarbonate, with an acidifying effect. With judicious use of intravenous saline therapy, these side effects can be avoided.



If administered sub-cutaneously, any addition to the isotonic solution could render it hypertonic and cause pain at the site of injection.



Administration of large doses may give rise to sodium accumulation, oedema, and hyperchloraemic acidosis.



4.9 Overdose



Injudicious intravenous saline therapy (e.g. post-operatively or in patients with impaired cardiac or renal function) may cause hypernatraemia. Osmotically induced water shift decreases intracellular volume, resulting in dehydration of internal organs, especially the brain, which may lead to thrombosis and haemorrhage. General adverse effects of sodium chloride excess in the body include: nausea, vomiting, diarrhoea, abdominal cramps, thirst, reduced salivary and lachrymal secretions, sweating, fever, hypotension, tachycardia, renal failure, peripheral and pulmonary oedema, respiratory arrest, headache, dizziness, restlessness, irritability, weakness, muscular twitching and rigidity, convulsions, coma and death. Excess chloride in the body may cause a loss of bicarbonate, with an acidifying effect.



With judicious use of intravenous saline therapy, these effects can be avoided.



Diuretics may be used to treat oedema resulting from isotonic expansion, and appropriate replacement therapy should be employed to avoid fluid and electrolyte imbalance. Treatment of hypervolaemic hypernatraemia requires removal of sodium in excess of water and can be achieved by replacing diuretic-induced sodium and water losses with only water. The basic aim of therapy is to restore the volume and composition of the body fluids to normal.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



The principal determinant of the effective osmolality of the extracellular fluids (and also of the intracellular fluids, since they remain in osmotic equilibrium with the extracellular fluids) is the extracellular fluid sodium concentration. The reason for this is because sodium is the most abundant positive ion of the extracellular fluid. Negative ion concentrations of the body fluids are adjusted to equal those of the positive ions by renal acid-base control mechanisms. Furthermore, glucose and urea, the most abundant of the non-ionic osmolar solutes in extracellular fluids, normally only represent about 3% of the total osmolality. Therefore, in effect, the extracellular fluid sodium ion concentration controls over 90% of the effective osmotic pressure of the extracellular fluid. Sodium chloride remains the most important single salt for prophylaxis or replacement therapy of deficits of extracellular fluid. Volume contraction, whether isotonic, hypotonic or hypertonic, may seriously impair the circulation (cardiac output falls and microcirculation is compromised) and prompt infusion of isotonic sodium chloride solution is indicated. Even with moderately severe hyponatraemia or hypernatraemia, the disorder may be corrected with isotonic saline solution, provided there is normal renal function to allow physiological adjustments to be made by the kidneys, resulting in the excretion of urine at a concentration appropriate to the underlying situation.



5.2 Pharmacokinetic Properties



The homeostatic mechanisms involved in maintaining constant ion concentrations are well described in standard text books of physiology and biochemistry and are not, therefore, included in this report.



5.3 Preclinical Safety Data



No further relevant information other than that which is contained in other sections of the Summary of Product Characteristics.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Dilute Hydrochloric acid B.P.



Water for Injections B.P.



6.2 Incompatibilities



The addition of sodium chloride to mannitol 20 or 25% may cause precipitation of the mannitol.



6.3 Shelf Life



3 years



6.4 Special Precautions For Storage



Do not store above 25°C



Keep in outer carton



6.5 Nature And Contents Of Container



2ml, 5ml and 10ml hermetically sealed translucent plastic ampoules, polypropylene Ph.Eur., packed in cardboard cartons to contain 10, 20, 50 and 100 ampoules.



6.6 Special Precautions For Disposal And Other Handling



For I.V. Injection



Solutions containing visible solid particles should not be used.



If only part of an ampoule is used, discard the remaining solution.



Use as directed by the physician.



Keep out of reach of children.



7. Marketing Authorisation Holder



Antigen International Ltd



Roscrea



Co. Tipperary



Ireland



8. Marketing Authorisation Number(S)



PL 02848/0157



9. Date Of First Authorisation/Renewal Of The Authorisation



11/ 10/1991



10. Date Of Revision Of The Text



22/02/2010




Tuesday, 1 May 2012

Cortalo with Aloe


Generic Name: hydrocortisone topical (hye droe KOR ti sone)

Brand Names: Ala-Cort, Ala-Scalp HP, Aquanil HC, Beta HC, Caldecort, Cortaid, Cortaid Intensive Therapy, Cortaid Maximum Strength, Cortaid with Aloe, Cortalo with Aloe, Corticaine, Cortizone for Kids, Cortizone-10, Cortizone-10 Intensive Healing Formula, Cortizone-10 Plus, Cortizone-5, Dermarest Dricort, Dermarest Eczema Medicated, Dermarest Plus Anti-Itch, Dermtex HC, Genasone/Aloe, Gly-Cort, Gynecort Maximum Strength, Hycort, Hydrocortisone 1% In Absorbase, Hydrocortisone with Aloe, Hydrocortisone-Aloe, Hytone, Instacort, Itch-X Lotion, Locoid, Locoid Lipocream, Locoid Lotion, Massengill Medicated Soft Cloth, MD Hydrocortisone, Neutrogena T-Scalp, NuCort with Aloe, NuZon, Pandel, Recort Plus, Rederm, Sarnol-HC, Scalacort, Texacort, U-Cort, Westcort


What is Cortalo with Aloe (hydrocortisone topical)?

Hydrocortisone is a topical steroid. It reduces the actions of chemicals in the body that cause inflammation, redness, and swelling.


Hydrocortisone topical is used to treat inflammation of the skin caused by a number of conditions such as allergic reactions, eczema, or psoriasis.


Hydrocortisone topical may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about Cortalo with Aloe (hydrocortisone topical)?


There are many brands and forms of hydrocortisone topical available and not all brands are listed on this leaflet.


Use this medication exactly as directed on the label, or as it has been prescribed by your doctor. Do not use the medication in larger amounts or for longer than recommended.


Do not cover treated skin areas with a bandage or other covering unless your doctor has told you to. If you are treating the diaper area of a baby, do not use plastic pants or tight-fitting diapers. Covering the skin that is treated with hydrocortisone topical can increase the amount of the drug your skin absorbs, which may lead to unwanted side effects. Follow your doctor's instructions.

Avoid using this medication on your face, near your eyes, or on body areas where you have skin folds or thin skin.


Do not use this medication on a child without a doctor's advice. Children are more sensitive to the effects of hydrocortisone topical.

Hydrocortisone topical will not treat a bacterial, fungal, or viral skin infection.


Contact your doctor if your condition does not improve or if it gets worse after using this medication for several days.

What should I discuss with my healthcare provider before using Cortalo with Aloe (hydrocortisone topical)?


Do not use this medication if you are allergic to hydrocortisone.

Hydrocortisone topical will not treat a bacterial, fungal, or viral skin infection.


FDA pregnancy category C. It is not known whether hydrocortisone topical is harmful to an unborn baby. Before using this medication, tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether hydrocortisone topical passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Do not use this medication on a child without a doctor's advice. Children are more sensitive to the effects of hydrocortisone topical.

How should I use Cortalo with Aloe (hydrocortisone topical)?


Use this medication exactly as directed on the label, or as it has been prescribed by your doctor. Do not use the medication in larger or smaller amounts, or use it for longer than recommended.


Hydrocortisone topical will not treat a bacterial, fungal, or viral skin infection.


Wash your hands before and after each application, unless you are using hydrocortisone topical to treat a hand condition.


Apply a small amount to the affected area and rub it gently into the skin.


Avoid using this medication on your face, near your eyes or mouth, or on body areas where you have skin folds or thin skin.


Do not cover treated skin areas with a bandage or other covering unless your doctor has told you to. If you are treating the diaper area of a baby, do not use plastic pants or tight-fitting diapers. Covering the skin that is treated with hydrocortisone topical can increase the amount of the drug your skin absorbs, which may lead to unwanted side effects. Follow your doctor's instructions. Contact your doctor if your condition does not improve or if it gets worse after using this medication for several days. It is important to use hydrocortisone topical regularly to get the most benefit. Store hydrocortisone topical at room temperature away from moisture and heat.

What happens if I miss a dose?


Use the medication as soon as you remember. If it is almost time for the next dose, skip the missed dose and use the medicine at the next regularly scheduled time. Do not use extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention if you think you have used too much of this medicine, or if anyone has accidentally swallowed it. An overdose of hydrocortisone topical applied to the skin is not expected to produce life-threatening symptoms.

What should I avoid while using Cortalo with Aloe (hydrocortisone topical)?


Avoid getting this medication in your eyes, mouth, and nose, or on your lips. If it does get into any of these areas, wash with water. Do not use hydrocortisone topical on sunburned, windburned, irritated, or broken skin. Also avoid using this medication in open wounds.

Avoid using skin products that can cause irritation, such as harsh soaps or shampoos or skin cleansers, hair coloring or permanent chemicals, hair removers or waxes, or skin products with alcohol, spices, astringents, or lime. Do not use other medicated skin products unless your doctor has told you to.


Cortalo with Aloe (hydrocortisone topical) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using hydrocortisone topical and call your doctor at once if you have any of these serious side effects:

  • blurred vision, or seeing halos around lights;




  • uneven heartbeats;




  • sleep problems (insomnia);




  • weight gain, puffiness in your face; or




  • feeling tired.



Less serious side effects may include:



  • skin redness, burning, itching, or peeling;




  • thinning of your skin;




  • blistering skin; or




  • stretch marks.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect Cortalo with Aloe (hydrocortisone topical)?


It is not likely that other drugs you take orally or inject will have an effect on topically applied hydrocortisone. But many drugs can interact with each other. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.



More Cortalo with Aloe resources


  • Cortalo with Aloe Side Effects (in more detail)
  • Cortalo with Aloe Use in Pregnancy & Breastfeeding
  • Cortalo with Aloe Drug Interactions
  • 0 Reviews for Cortalo with Aloe - Add your own review/rating


  • Anusol-HC Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Carmol HC Prescribing Information (FDA)

  • Carmol HC MedFacts Consumer Leaflet (Wolters Kluwer)

  • CortAlo With Aloe Advanced Consumer (Micromedex) - Includes Dosage Information

  • Cortizone-10 Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Hydrocortisone Acetate Monograph (AHFS DI)

  • Hydrocortisone with Aloe Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Hytone Prescribing Information (FDA)

  • Instacort Gel MedFacts Consumer Leaflet (Wolters Kluwer)

  • Locoid Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Locoid Lipocream Prescribing Information (FDA)

  • Locoid Lotion Prescribing Information (FDA)

  • Nutracort Lotion MedFacts Consumer Leaflet (Wolters Kluwer)

  • Pandel Prescribing Information (FDA)

  • Pediaderm HC Lotion MedFacts Consumer Leaflet (Wolters Kluwer)

  • ProctoCream-HC Cream MedFacts Consumer Leaflet (Wolters Kluwer)

  • Proctocort Prescribing Information (FDA)

  • Texacort Prescribing Information (FDA)

  • U-cort Prescribing Information (FDA)

  • Westcort Prescribing Information (FDA)



Compare Cortalo with Aloe with other medications


  • Anal Itching
  • Aphthous Stomatitis, Recurrent
  • Atopic Dermatitis
  • Dermatitis
  • Eczema
  • Gingivitis
  • Hemorrhoids
  • Proctitis
  • Pruritus
  • Psoriasis
  • Seborrheic Dermatitis
  • Skin Rash


Where can I get more information?


  • Your pharmacist can provide more information about hydrocortisone topical.

See also: Cortalo with Aloe side effects (in more detail)