Razadyne Side Effects

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Razadyne Safety Reports

Total Razadyne reports: 46.
Razadyne FDA safety alerts: No.
Reported deaths: 8    Reported hospitalizations: 21.
Take Razadyne Side Effects Survey or Share Your Razadyne Story.
Reported Razadyne Side Effects: confusional state, hallucination, visual, cerebrovascular accident, pulmonary mass, cough, aggression, insomnia, dyskinesia, death, headache, lethargy.
Razadyne Usage.

Razadyne Side Effects Report #5199683-0
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Dec 27, 2006. Male patient, weighting 180.0 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage, decubitus ulcer, osteomyelitis. RAZADYNE dosage: unknown. During the same period patient was treated with NAMENDA, ADVAIR DISKUS, ALBUTEROL. Patient died on 10/18/2006.

Razadyne Side Effects Report #5211606-4
RAZADYNE problem was reported by a Health Professional from UNITED STATES on Jan 08, 2007. Male patient, 87 years of age, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: syncope. RAZADYNE dosage: unknown. During the same period patient was treated with NAMENDA, LANSOPRAZOLE, LEVOTHYROXINE, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5313226-X
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Dec 13, 2006. Female patient, 80 years of age, weighting 122.0 lb, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: somnolence, speech disorder, urinary tract infection. RAZADYNE dosage: 24 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with NAMENDA, FLOMAX, FOSAMAX. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5313227-1
RAZADYNE problem was reported by a Physician from UNITED STATES on Nov 22, 2006. Male patient, 73 years of age, weighting 175.0 lb, was diagnosed with dementia and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: hallucination, visual, malaise, nausea, vertigo. RAZADYNE dosage: unknown. During the same period patient was treated with RAZADYNE ER, SOTALOL, PREDNISONE, SINEMET CR, FLORINEF. Patient recovered.

Razadyne Side Effects Report #5313228-3
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Oct 11, 2006. Male patient, 84 years of age, weighting 175.0 lb, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: bradycardia, hyperhidrosis, hypokinesia, tremor. RAZADYNE dosage: unknown. During the same period patient was treated with LOPRESSOR, PROVIGIL, HYZAAR, BABY ASA. Patient recovered.

Razadyne Side Effects Report #5313229-5
RAZADYNE problem was reported by a Physician from UNITED STATES on Oct 13, 2006. Female patient was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: hallucination. RAZADYNE dosage: unknown. Patient recovered.

Razadyne Side Effects Report #5313240-4
Physician from UNITED STATES reported RAZADYNE problem on Dec 21, 2006. Male patient, 84 years of age, weighting 170.0 lb, was diagnosed with dementia, dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, confusional state, dyskinesia, lethargy. RAZADYNE dosage: 8 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with RAZADYNE ER, VASOTEC, PRAVACHOL, COREG, COUMADIN, TOPROL, PROSCAR, LASIX. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5232305-9
RAZADYNE problem was reported by a Physician from UNITED STATES on Feb 01, 2007. Female patient, weighting 122.0 lb, was diagnosed with memory impairment, sinus disorder, sleep disorder and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: ankle fracture, condition aggravated, insomnia. RAZADYNE dosage: unknown. During the same period patient was treated with RAZADYNE ER, PREDNISONE, AMBIEN. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5239410-1
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Feb 06, 2007. Female patient, weighting 253.0 lb, was diagnosed with insomnia, weight decreased, blood cholesterol increased, thyroid disorder, contraception and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: headache, incontinence, insomnia. RAZADYNE dosage: unknown. During the same period patient was treated with ROZEREM, TOPAMAX, NYASPAN, SYNTHROID, YASMIN. Patient recovered.

Razadyne Side Effects Report #5243663-3
RAZADYNE problem was reported by a Physician from UNITED STATES on Feb 15, 2007. Female patient, weighting 122.0 lb, was diagnosed with memory impairment, sinus disorder, sleep disorder and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: ankle fracture, insomnia. RAZADYNE dosage: unknown. During the same period patient was treated with RAZADYNE ER, PREDNISONE, AMBIEN. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5260822-4
Physician from UNITED STATES reported RAZADYNE problem on Mar 01, 2007. Female patient, weighting 253.0 lb, was diagnosed with insomnia, migraine, weight decreased, blood cholesterol increased, thyroid disorder, contraception, multiple allergies and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: headache, incontinence, insomnia. RAZADYNE dosage: unknown. During the same period patient was treated with ROZEREM, TOPAMAX, NYASPAN, SYNTHROID, YASMIN, SINGULAIR. Patient recovered.

Razadyne Side Effects Report #5262359-5
RAZADYNE problem was reported by a Pharmacist from UNITED STATES on Mar 09, 2007. Male patient was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: convulsion, loss of consciousness. RAZADYNE dosage: 24 MG QD PO. During the same period patient was treated with LIPITOR, PROZAC, SYNTHROID. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5272618-8
Physician from UNITED STATES reported RAZADYNE problem on Mar 20, 2007. Female patient, 80 years of age, weighting 165.0 lb, was diagnosed with dementia and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: hypotension, sinus bradycardia. RAZADYNE dosage: unknown. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5345835-6
RAZADYNE problem was reported by a Physician from UNITED STATES on Nov 22, 2006. Male patient, 73 years of age, weighting 175.0 lb, was diagnosed with dementia and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: hallucination, visual, malaise, nausea, vertigo. RAZADYNE dosage: unknown. During the same period patient was treated with RAZADYNE ER, SOTALOL, PREDNISONE, SINEMET CR, FLORINEF. Patient recovered.

Razadyne Side Effects Report #5345842-3
Physician from UNITED STATES reported RAZADYNE problem on July 27, 2006. Female patient, 90 years of age, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: aggression, confusional state. RAZADYNE dosage: 8 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with NAMENDA. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5345851-4
RAZADYNE problem was reported by a Physician from UNITED STATES on Dec 21, 2006. Male patient, 84 years of age, weighting 170.0 lb, was diagnosed with dementia, dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, confusional state, dyskinesia, lethargy. RAZADYNE dosage: 8 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with RAZADYNE ER, VASOTEC, PRAVACHOL, COREG, COUMADIN, TOPROL, PROSCAR, LASIX. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5345854-X
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Mar 07, 2006. Male patient, 61 years of age, weighting 250.0 lb, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: depressed mood, suicidal ideation. RAZADYNE dosage: 8 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with ARICEPT, EFFEXOR, LAVASTATIN, HYTRIN, AUGMENTIN. Patient recovered.

Razadyne Side Effects Report #5345858-7
RAZADYNE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 01, 2006. Female patient, 86 years of age, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage. RAZADYNE dosage: unknown. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5345869-1
Physician from UNITED STATES reported RAZADYNE problem on Mar 20, 2006. Female patient, 80 years of age, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident. RAZADYNE dosage: 12 MG, 1 IN 1 DAY. During the same period patient was treated with NAMENDA. Patient was hospitalized and became disabled. Patient recovered.

Razadyne Side Effects Report #5345874-5
RAZADYNE problem was reported by a Physician from UNITED STATES on Jan 02, 2007. Male patient, 75 years of age, weighting 190.0 lb, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: aggression, paranoia. RAZADYNE dosage: 4 MG, 2 IN 1 DAY, ORAL. During the same period patient was treated with PROZAC, TRAZODONE, ATENOLOL, METHADONE, COUMADIN. Patient recovered.

Razadyne Side Effects Report #5345880-0
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Dec 13, 2006. Female patient, 80 years of age, weighting 122.0 lb, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: somnolence, speech disorder, urinary tract infection. RAZADYNE dosage: 24 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with NAMENDA, FLOMAX, FOSAMAX. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5345882-4
RAZADYNE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 28, 2006. Female patient, 88 years of age, weighting 120.0 lb, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: myocardial infarction. RAZADYNE dosage: unknown. During the same period patient was treated with TOPROL, NAMENDA, PRAVACHOL, BABY ASPIRIN. Patient died on 10/27/2006.

Razadyne Side Effects Report #5345933-7
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Oct 25, 2006. Female patient, 88 years of age, weighting 145.0 lb, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: feeling abnormal, headache, regressive behaviour, sleep disorder, weight decreased. RAZADYNE dosage: 8 MG, 2 IN 1 DAY, ORAL. During the same period patient was treated with NAMENDA, SPIROLACTONE, PREMARIN. Patient recovered.

Razadyne Side Effects Report #5345973-8
RAZADYNE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 11, 2006. Male patient, 84 years of age, weighting 175.0 lb, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: bradycardia, hyperhidrosis, hypokinesia, tremor. RAZADYNE dosage: unknown. During the same period patient was treated with LOPRESSOR, PROVIGIL, HYZAAR, BABY ASA. Patient recovered.

Razadyne Side Effects Report #5345978-7
Physician from UNITED STATES reported RAZADYNE problem on Oct 13, 2006. Female patient was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: hallucination. RAZADYNE dosage: unknown. Patient recovered.

Razadyne Side Effects Report #5346002-2
RAZADYNE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 30, 2006. Male patient, 77 years of age, weighting 180.0 lb, was diagnosed with dementia and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: heart rate decreased. RAZADYNE dosage: 8 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with PLAVIX, ASPIRIN, GLYBURIDE, GLUCOPHAGE, HYDROCHLOROTHIAZIDE, OMEPRAZOLE, PROPRANOLOL, QUINAPRIL. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5346022-8
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Nov 14, 2006. Female patient, 65 years of age, weighting 230.0 lb, was diagnosed with memory impairment and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: blood pressure increased. RAZADYNE dosage: 4 MG, 2 IN 1 DAY, ORAL. During the same period patient was treated with ZALATAN, SYNTHROID, ZETIA. Patient recovered.

Razadyne Side Effects Report #5346025-3
RAZADYNE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 18, 2006. Female patient, 76 years of age, weighting 125.0 lb, was diagnosed with blood pressure, dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: akathisia, anorexia, dizziness, psychomotor hyperactivity. RAZADYNE dosage: 16 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with RAZADYNE ER, TRI HYDROCHLOROTHIAZIDE. Patient recovered.

Razadyne Side Effects Report #5370085-7
Physician from FRANCE reported RAZADYNE problem on June 14, 2007. Male patient, 79 years of age, was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: intestinal obstruction. RAZADYNE dosage: unknown. During the same period patient was treated with MOCLAMINE. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5370086-9
RAZADYNE problem was reported by a Consumer or non-health professional from BRAZIL on June 14, 2007. Female patient, 83 years of age, weighting 169.8 lb, was diagnosed with dementia alzheimer's type, hypertension, diabetes mellitus, prophylaxis and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: bone operation, diarrhoea. RAZADYNE dosage: unknown. During the same period patient was treated with RAZADYNE ER, NATRILIX, OROXADIN, ATENOLOL, GLUCOVANCE, NAPRIX, ASPIRIN. Patient recovered.

Razadyne Side Effects Report #5066304-7
Physician from UNITED STATES reported RAZADYNE problem on June 07, 2006. Female patient, 90 years of age, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: aggression, confusional state. RAZADYNE dosage: 8 MG, 1 IN 1 DAY, ORAL. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5072447-4
RAZADYNE problem was reported by a Consumer or non-health professional from UNITED STATES on July 27, 2006. Male patient, weighting 180.0 lb, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: renal failure. RAZADYNE dosage: unknown. During the same period patient was treated with NAMENDA. Patient died on 06/09/2006.

Razadyne Side Effects Report #5101527-X
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Sept 01, 2006. Male patient, weighting 180.0 lb, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: renal failure. RAZADYNE dosage: unknown. During the same period patient was treated with NAMENDA. Patient died on 06/09/2006.

Razadyne Side Effects Report #5130676-5
RAZADYNE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 10, 2006. Female patient, weighting 105.0 lb, was diagnosed with dementia alzheimer's type, blood pressure abnormal, coagulopathy and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cough, pulmonary mass. RAZADYNE dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, FOSAMAX, EVISTA, MIACALCIN, HYDROCHLOROTHIAZIDE, NABUMETONE, ASPIRIN. Patient recovered.

Razadyne Side Effects Report #5202520-9
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Sept 08, 2006. Male patient, 84 years of age, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, dyskinesia. RAZADYNE dosage: unknown. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5202522-2
RAZADYNE problem was reported by a Physician from UNITED STATES on July 27, 2006. Female patient, 90 years of age, was diagnosed with dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: aggression, confusional state. RAZADYNE dosage: 8 MG, 1 IN 1 D, ORAL. During the same period patient was treated with NAMENDA. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5145117-1
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on Oct 31, 2006. Male patient, weighting 180.0 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage, decubitus ulcer, osteomyelitis. RAZADYNE dosage: unknown. During the same period patient was treated with NAMENDA, ADVAIR DISKUS, ALBUTEROL. Patient died on 10/18/2006.

Razadyne Side Effects Report #5145826-4
RAZADYNE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 31, 2006. Male patient, weighting 136.0 lb, was diagnosed with dementia and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: coronary arterial stent insertion, pneumonia. RAZADYNE dosage: unknown. During the same period patient was treated with ZOCOR, ASPIRIN, ZYRTEC, PLAVIX, TOPROL, ALTACE, PEPCID, MICARDIS. Patient was hospitalized. Patient died on 02/25/2006.

Razadyne Side Effects Report #5145939-7
Physician from UNITED STATES reported RAZADYNE problem on Oct 30, 2006. Female patient, weighting 105.0 lb, was diagnosed with dementia alzheimer's type, blood pressure abnormal, coagulopathy and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cough, pulmonary mass. RAZADYNE dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, FOSAMAX, EVISTA, MIACALCIN, HYDROCHLOROTHIAZIDE, NABUMETONE, ASPIRIN. Patient recovered.

Razadyne Side Effects Report #5146781-3
RAZADYNE problem was reported by a Physician from UNITED STATES on Nov 02, 2006. Female patient, weighting 105.0 lb, was diagnosed with dementia alzheimer's type, hypertension, osteoporosis, osteoarthritis and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cough, pulmonary mass. RAZADYNE dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, FOSAMAX, EVISTA, MIACALCIN, HYDROCHLOROTHIAZIDE, RELAFEN. Patient recovered.

Razadyne Side Effects Report #5155190-2
Physician from UNITED STATES reported RAZADYNE problem on Nov 14, 2006. Female patient, weighting 105.0 lb, was diagnosed with dementia alzheimer's type, hypertension, osteoporosis, osteoarthritis and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cough, multiple myeloma, pleural fibrosis, pneumothorax, pulmonary mass. RAZADYNE dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, FOSAMAX, EVISTA, MIACALCIN, HYDROCHLOROTHIAZIDE, RELAFEN. Patient recovered.

Razadyne Side Effects Report #5383873-8
RAZADYNE problem was reported by a Consumer or non-health professional from UNITED STATES on June 29, 2007. Male patient, 88 years of age, weighting 175.0 lb, was diagnosed with memory impairment, pain, blood cholesterol increased, eye disorder, abnormal faeces and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: delusion, hallucination, logorrhoea, pneumonia, rib fracture, sleep disorder, somnolence, stupor. RAZADYNE dosage: unknown. During the same period patient was treated with RAZADYNE ER, TYLOX, DIPYRIDAMOL, RANITIDINE, SIMVASTATIN, ASA BABY, EYE CAPS, DOCUSATE. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5403858-2
Consumer or non-health professional from UNITED STATES reported RAZADYNE problem on July 31, 2007. Female patient, 85 years of age, weighting 135.0 lb, was diagnosed with dementia and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, blood pressure increased, hallucination, nausea, pyrexia, speech disorder, transient ischaemic attack, vomiting. RAZADYNE dosage: 8 MG ONCE A DAY. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5413273-3
RAZADYNE problem was reported by a Physician from UNITED STATES on Apr 05, 2007. Male patient, 84 years of age, weighting 170.0 lb, was diagnosed with dementia, dementia alzheimer's type and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, confusional state, dyskinesia, lethargy. RAZADYNE dosage: 8 MG, 1 IN 1 DAY, ORAL. During the same period patient was treated with RAZADYNE ER, VASOTEC, PRAVACHOL, COREG, COUMADIN, TOPROL, PROSCAR, LASIX. Patient was hospitalized. Patient recovered.

Razadyne Side Effects Report #5429447-1
Physician from BRAZIL reported RAZADYNE problem on Aug 20, 2007. Male patient, 79 years of age, weighting 141.1 lb, was diagnosed with dementia alzheimer's type, parkinson's disease, cardiac failure, urinary tract infection, vitamin supplementation, cardiovascular disorder and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: apathy, prostration. RAZADYNE dosage: unknown. During the same period patient was treated with PROLOPA, ALDAZIDA, DIVELOL, MACRODANTINA, ASPIRIN, BENERVA, REMERON, GINKO BILOBA. Patient died on 12/01/2006.

Razadyne Side Effects Report #5450281-0
RAZADYNE problem was reported by a Physician from UNITED STATES on Sept 04, 2007. Male patient, weighting 184.0 lb, was diagnosed with dementia, blood cholesterol, cerebrovascular accident, neuropathy peripheral, gastrooesophageal reflux disease and was treated with RAZADYNE. After drug was administered, patient experienced the following problems/side effects: face injury. RAZADYNE dosage: unknown. During the same period patient was treated with ARICEPT, LIPITOR, PLAVIX, CARBATROL, ACIPHEX. Patient died on 08/23/2007.


Drug Information: Galantamine

URL of this page: http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a699058.html

(ga lan' ta meen)

Why is this medication prescribed?

Galantamine is used to treat the symptoms of Alzheimer's disease (AD; a brain disease that slowly destroys the memory and the ability to think, learn, communicate and handle daily activities). Galantamine is in a class of medications called acetylcholinesterase inhibitors. It works by increasing the amount of a certain natural substance in the brain that is needed for memory and thought. Galantamine may improve the ability to think and remember or slow the loss of these abilities in people who have AD. However, galantamine will not cure AD or prevent the loss of mental abilities at some time in the future.

How should this medicine be used?

Galantamine comes as a tablet, an extended-release (long-acting) capsule, and a solution (liquid) to take by mouth. The tablets and liquid are usually taken twice a day, preferably with the morning and evening meals. The extended-release capsules are usually taken once a day in the morning. Take galantamine at around the same time(s) every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take galantamine exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor. You are less likely to experience side effects of galantamine if you follow the exact dosing schedule prescribed by your doctor.

Galantamine may upset your stomach, especially at the beginning of your treatment. Take galantamine with food and drink 6-8 glasses of water every day. This may decrease the chance that you will have an upset stomach during your treatment.

Your doctor will probably start you on a low dose of galantamine and gradually increase your dose, not more often than once every 4 weeks.

Continue to take galantamine even if you feel well. Do not stop taking galantamine without talking to your doctor. If you do stop taking galantamine for a few days or longer, call your doctor before you start to take galantamine again. Your doctor will probably tell you to start with the lowest dose of galantamine and gradually increase your dose to the dose you had been taking.

Before you take galantamine oral solution for the first time, read the written instructions that come with it. Ask your doctor or pharmacist to show you how to take the oral solution. To take the oral solution, follow these steps:

  • Open the child-proof cap by pushing the cap down while turning it to the left. Remove the cap.
  • Pull the pipette (the tube that you use to measure the dose of galantamine) out of its case.
  • Place the pipette fully into the bottle of galantamine.
  • While holding the bottom ring of the pipette, pull the pipette plunger up to the marking that shows the dose your doctor prescribed.
  • Hold the bottom ring of the pipette and remove the pipette from the bottle. Be careful not to push the plunger in.
  • Prepare 3-4 ounces (about 1/2 cup) of any non-alcoholic drink. Empty all the medicine from the pipette into the drink by pushing the plunger all the way in.
  • Stir the drink well.
  • Drink all of the mixture right away.
  • Put the plastic cap back on the bottle of galantamine and turn the cap to the right to close the bottle.
  • Rinse the empty pipette by putting its open end into a glass of water, pulling the plunger out, and pushing the plunger in to remove the water.

Other uses for this medicine

This medication may be prescribed for other uses; ask your doctor or pharmacist for more information.

What special precautions should I follow?

Before taking galantamine,

  • tell your doctor and pharmacist if you are allergic to galantamine, any other medications, or any of the inactive ingredients in galantamine tablets, solution, or extended-release capsules. Ask your pharmacist for a list of the inactive ingredients.
  • tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Be sure to mention any of the following: ambenonium chloride (Mytelase); amitriptyline (Elavil); anticholinergic medications such as atropine (Atropen, Sal-Tropine), belladonna (in Donnatal, Bellamine, Bel-Tabs, others); benztropine (Cogentin), biperiden (Akineton); clidinium (in Librax), dicyclomine (Bentyl), glycopyrrolate (Robinul), hyoscyamine (Cytospaz-M, Levbid, Levsin), ipratropium (Atrovent, in Combivent), oxybutynin (Ditropan), procyclidine (Kemadrin), propantheline (Pro-Banthine), scopolamine (Scopace, Transderm-Scop), tiotropium (Spiriva), tolterodine (Detrol), and trihexyphenidyl;certain antifungals such as fluconazole (Diflucan), itraconazole (Sporanox), ketoconazole (Nizoral), and voriconazole (Vfend);aspirin or other nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen (Advil, Motrin) and naproxen (Aleve, Naprosyn); bethanechol (Urecholine);cevimeline (Evoxac); cimetidine (Tagamet); clarithromycin (Biaxin, in Prevpac);digoxin (Lanoxin); fluoxetine (Prozac, Sarafem); fluvoxamine (Luvox); heart medications; nefazodone; neostigmine (Prostigmin); other medications for Alzheimer's disease; medications for human immunodeficiency syndrome (HIV) or acquired immunodeficiency syndrome (AIDS); medications for high blood pressure; paroxetine (Paxil); pyridostigmine (Mestinon); and quinidine (Quinidex). Your doctor may need to change the doses of your medications or monitor you carefully for side effects.
  • tell your doctor if you have or have ever had asthma or any other lung disease; an enlarged prostate; ulcers; seizures; irregular heartbeat;or heart, kidney, or liver disease.
  • tell your doctor if you are pregnant, plan to become pregnant, or are breast-feeding. If you become pregnant while taking galantamine, call your doctor.
  • if you are having surgery, including dental surgery, tell the doctor or dentist that you are taking galantamine.
  • you should know that galantamine may make you drowsy. Do not drive a car or operate machinery until you know how this medication affects you.
  • remember that alcohol can add to the drowsiness caused by this medication.

What special dietary instructions should I follow?

Unless your doctor tells you otherwise, continue your normal diet.

What should I do if I forget a dose?

Take the missed dose as soon as you remember it. However, if it is almost time for the next dose, skip the missed dose and continue your regular dosing schedule. Do not take a double dose to make up for a missed one.

What side effects can this medication cause?

Galantamine may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:

  • upset stomach
  • vomiting
  • diarrhea
  • loss of appetite
  • stomach pain
  • heartburn
  • weight loss
  • extreme tiredness
  • dizziness
  • pale skin
  • headache
  • shaking of a part of your body that you cannot control
  • depression
  • difficulty falling asleep or staying asleep
  • runny nose

Some side effects can be serious. The following symptoms are uncommon, but if you experience any of them, call your doctor immediately:

  • difficulty urinating
  • blood in the urine
  • pain or burning while urinating
  • seizures
  • slowed heartbeat
  • fainting
  • shortness of breath
  • black and tarry stools
  • red blood in the stools
  • bloody vomit
  • vomiting material that looks like coffee grounds

Galantamine may cause other side effects. Call your doctor if you have any unusual problems while taking this medication.

If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online [at http://www.fda.gov/MedWatch/index.html] or by phone [1-800-332-1088].

What storage conditions are needed for this medicine?

Keep this medication in the container it came in, tightly closed, and out of reach of children. Store it at room temperature and away from excess heat and moisture (not in the bathroom). Do not freeze. Throw away any medication that is outdated or no longer needed. Talk to your pharmacist about the proper disposal of your medication.

In case of emergency/overdose

In case of overdose, call your local poison control center at 1-800-222-1222. If the victim has collapsed or is not breathing, call local emergency services at 911.

Symptoms of overdose may include:

  • muscle weakness or twitching
  • upset stomach
  • vomiting
  • stomach cramps
  • drooling
  • teary eyes
  • increased urination
  • need to have a bowel movement
  • sweating
  • slowed, fast, or irregular heartbeat
  • lightheadedness
  • dizziness
  • fainting
  • slowed breathing
  • collapse
  • loss of conciousness
  • seizures
  • dry mouth
  • chest pain
  • hallucinations (seeing things or hearing voices that do not exist)

What other information should I know?

Keep all appointments with your doctor.

Do not let anyone else take your medication. Ask your pharmacist any questions you have about refilling your prescription.

It is important for you to keep a written list of all of the prescription and nonprescription (over-the-counter) medicines you are taking, as well as any products such as vitamins, minerals, or other dietary supplements. You should bring this list with you each time you visit a doctor or if you are admitted to a hospital. It is also important information to carry with you in case of emergencies.

Brand name(s):

  • Razadyne® (formerly available as Reminyl®)
  • Razadyne ®ER

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PatientsVille.com does not provide medical advice, diagnosis or treatment. The information contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments.


Thank you for visiting Patientsville.com. We hope you found our information about prescription drug side effects helpful. The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Thank you for visiting Patientsville.net. Hope you enjoyed finding Razadyne safety information and found answers to Your Questions about Razadyne side effects