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Singulair Side Effects Report #5690629-5
Consumer or non-health professional from UNITED STATES reported SINGULAIR problem on Mar 31, 2008. Male patient, 53 years of age, weighting 290.0 lb, was diagnosed with hypersensitivity and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: decreased activity, depression, hypersomnia, lethargy, . SINGULAIR dosage: 5 MG -? HALF DOSE- DAILY PO. Patient recovered.

Tracleer Side Effects Report #5632706-0
TRACLEER problem was reported by a Physician from UNITED STATES on Feb 01, 2008. Male patient, 81 years of age, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: decreased activity, dysuria, feeling abnormal, malaise, oedema peripheral, pulmonary embolism, thrombosis, urinary retention, urine flow decreased, . TRACLEER dosage: 62.5 MG, BID, ORAL. Patient was hospitalized. Patient recovered.

Sevredol Side Effects Report #5581593-8
Pharmacist from SPAIN reported SEVREDOL problem on Dec 28, 2007. Male patient, 76 years of age, was diagnosed with post herpetic neuralgia and was treated with SEVREDOL. After drug was administered, patient experienced the following problems/side effects: decreased activity, dyspnoea, somnolence, . SEVREDOL dosage: 10 MG, 12 TABLETS. During the same period patient was treated with SPIRIVA, SERETIDE, ACETYLCYSTEINE, CIPROFLOXACIN. Patient was hospitalized. Patient recovered.

Actos Side Effects Report #5572315-5
ACTOS problem was reported by a Consumer or non-health professional from GERMANY on Dec 10, 2007. Female patient, 79 years of age, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: decreased activity, humerus fracture, hyperglycaemia, pain, . ACTOS dosage: 30 MG (30 MG, 1 - 0 - 0 TABLET PER ORAL. During the same period patient was treated with METFORMIN, ACETYLSALICYLIC ACID SRT, RAMIPRIL, METOPROLOL SUCCINATE, SIMVA. Patient was hospitalized and became disabled. Patient recovered.


Bextra Side Effects Report #5596304-X
Consumer or non-health professional from UNITED STATES reported BEXTRA problem on Apr 16, 2007. Female patient, 69 years of age, was diagnosed with nerve injury, pain and was treated with BEXTRA. After drug was administered, patient experienced the following problems/side effects: decreased activity, depression, gastrointestinal disorder, nausea, obesity, . BEXTRA dosage: unknown. During the same period patient was treated with CELEBREX, DARVOCET, CHLORTHALIDONE, PAXIL. Patient recovered.

Duloxetine Side Effects Report #5509961-0
DULOXETINE problem was reported by a Physician from UNITED STATES on Nov 07, 2007. Female patient, 65 years of age, weighting 200.0 lb, was diagnosed with major depression, pain and was treated with DULOXETINE. After drug was administered, patient experienced the following problems/side effects: decreased activity, disturbance in attention, dyspnoea exertional, hypertension, impaired work ability, malaise, tachycardia, wheezing, . DULOXETINE dosage: 10-60MG DAILY PO. During the same period patient was treated with LISINOPRIL, AMLODIPINE, HYDROCHLOROTHIAZIDE, PROPRANOLOL, METOPROLOL TARTRATE, HYDRALAZINE. Patient recovered.

Risperdal Side Effects Report #5513125-4
Physician from GERMANY reported RISPERDAL problem on Nov 06, 2007. Female patient, weighting 132.3 lb, was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: decreased activity, hypotension, intentional overdose, suicide attempt, tachycardia, . RISPERDAL dosage: unknown. Patient recovered.

Coreg Side Effects Report #5515640-6
COREG problem was reported by a Consumer or non-health professional from UNITED STATES on July 19, 2007. Female patient, 79 years of age, was diagnosed with hypertension and was treated with COREG. After drug was administered, patient experienced the following problems/side effects: decreased activity, feeling abnormal, sluggishness, . COREG dosage: unknown. During the same period patient was treated with PAROXETINE, PAXIL. Patient recovered.

Forteo Side Effects Report #5522220-5
Consumer or non-health professional from UNITED STATES reported FORTEO problem on Nov 06, 2007. Female patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: decreased activity, fall, injection site haemorrhage, lower limb fracture, muscular weakness, pelvic fracture, resorption bone increased, upper limb fracture, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.


Chantix Side Effects Report #5525837-7
CHANTIX problem was reported by a Physician from UNITED STATES on Nov 14, 2007. Female patient, weighting 89.95 lb, was diagnosed with tobacco abuse and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: decreased activity, depressed mood, treatment noncompliance, . CHANTIX dosage: unknown. Patient recovered.

Rozerem Side Effects Report #5529029-7
Consumer or non-health professional from UNITED STATES reported ROZEREM problem on Oct 12, 2007. Male patient, 57 years of age, weighting 237.0 lb, was diagnosed with insomnia, middle insomnia and was treated with ROZEREM. After drug was administered, patient experienced the following problems/side effects: decreased activity, hangover, middle insomnia, . ROZEREM dosage: 8 MG, QHS, PER ORAL. Patient recovered.

Pimozide Side Effects Report #5530408-2
PIMOZIDE problem was reported by a Consumer or non-health professional from GERMANY on Nov 15, 2007. Male patient, 21 years of age, was treated with PIMOZIDE. After drug was administered, patient experienced the following problems/side effects: decreased activity, suicide attempt, . PIMOZIDE dosage: unknown. During the same period patient was treated with TIAPRIDE HYDROCHLORIDE, ZOPICLONE. Patient recovered.

Byetta Side Effects Report #5577728-3
Consumer or non-health professional from UNITED STATES reported BYETTA problem on June 22, 2007. Male patient, 65 years of age, was diagnosed with insulin resistant diabetes and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: decreased activity, decreased appetite, feeling abnormal, headache, . BYETTA dosage: unknown. Patient recovered.

Luvox Side Effects Report #5489571-4
LUVOX problem was reported by a Pharmacist from UNITED STATES on Oct 16, 2007. Female patient, 60 years of age, weighting 198.4 lb, was treated with LUVOX. After drug was administered, patient experienced the following problems/side effects: decreased activity, incontinence, serotonin syndrome, . LUVOX dosage: 200 MG BID PO. During the same period patient was treated with TOPAMAX. Patient was hospitalized. Patient recovered.


Myozyme Side Effects Report #5502311-5
Health Professional from UNITED STATES reported MYOZYME problem on Oct 15, 2007. Male patient, 42 years of age, weighting 152.1 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: decreased activity, disease progression, glycogen storage disease type ii, vital capacity decreased, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with TENORMIN, PLENDIL. Patient recovered.

Champix Side Effects Report #5453122-0
CHAMPIX problem was reported by a Health Professional from UNITED KINGDOM on Sept 04, 2007. Female patient, 32 years of age, weighting 140.0 lb, was diagnosed with contraception and was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: decreased activity, impaired work ability, nausea, vomiting, . CHAMPIX dosage: unknown. During the same period patient was treated with LOESTRIN. Patient recovered.

Humira Side Effects Report #5453167-0
Consumer or non-health professional from CANADA reported HUMIRA problem on Sept 04, 2007. Male patient, weighting 170.2 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: decreased activity, sepsis, . HUMIRA dosage: unknown. Patient died on 08/21/2007.

Avelox Side Effects Report #5462960-X
AVELOX problem was reported by a Consumer or non-health professional from BELGIUM on Sept 17, 2007. Male patient, 41 years of age, was diagnosed with bronchitis and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: decreased activity, . AVELOX dosage: UNIT DOSE: 400 MG. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5404048-X
Consumer or non-health professional from UNITED STATES reported FORTEO problem on July 23, 2007. Female patient, 86 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: decreased activity, fall, injection site haemorrhage, muscular weakness, pelvic fracture, upper limb fracture, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.


Cymbalta Side Effects Report #5407471-2
CYMBALTA problem was reported by a Physician from UNITED STATES on July 25, 2007. Female patient, 85 years of age, was diagnosed with depression and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: decreased activity, drooling, flat affect, lack of spontaneous speech, tardive dyskinesia, . CYMBALTA dosage: 60 MG, UNK. During the same period patient was treated with ARICEPT, NAMENDA, PLAVIX, XANAX, FOLIC ACID, TOPROL. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5431587-8
Consumer or non-health professional from CANADA reported HUMIRA problem on Aug 24, 2007. Male patient, weighting 170.2 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: decreased activity, pneumonia, . HUMIRA dosage: unknown. Patient died on 08/21/2007.

Humira Side Effects Report #5437390-7
HUMIRA problem was reported by a Consumer or non-health professional from CANADA on Aug 24, 2007. Male patient, weighting 170.2 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: decreased activity, mobility decreased, pneumonia, . HUMIRA dosage: unknown. Patient died on 08/21/2007.

Zyprexa Side Effects Report #5387459-0
Physician from JAPAN reported ZYPREXA problem on July 02, 2007. Female patient, 51 years of age, weighting 179.1 lb, was diagnosed with schizophrenia and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: decreased activity, increased appetite, metabolic syndrome, weight increased, . ZYPREXA dosage: unknown. Patient was hospitalized. Patient recovered.

Procrit Side Effects Report #5398360-0
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2007. Male patient, weighting 165.1 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: decreased activity, fatigue, feeling abnormal, . PROCRIT dosage: unknown. During the same period patient was treated with ZOCOR. Patient recovered.

Zyprexa Side Effects Report #5387459-0
Physician from JAPAN reported ZYPREXA problem on July 02, 2007. Female patient, 51 years of age, weighting 179.1 lb, was diagnosed with schizophrenia and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: decreased activity, increased appetite, metabolic syndrome, weight increased, . ZYPREXA dosage: unknown. Patient was hospitalized. Patient recovered.

Procrit Side Effects Report #5398360-0
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2007. Male patient, weighting 165.1 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: decreased activity, fatigue, feeling abnormal, . PROCRIT dosage: unknown. During the same period patient was treated with ZOCOR. Patient recovered.

Aricept Side Effects Report #5767991-8
Physician from JAPAN reported ARICEPT problem on June 04, 2008. Female patient, 79 years of age, was diagnosed with dementia alzheimer's type and was treated with ARICEPT. After drug was administered, patient experienced the following problems/side effects: decreased activity, dementia, fall, torticollis, wrist fracture, . ARICEPT dosage: 5 MG, 1 IN 1 D, ORAL : 7.5 MG, 1 IN 1 D, ORAL : 10 MG, 1 IN 1 D, ORAL. During the same period patient was treated with LOCHOL, LIPITOR, SELBEX. Patient was hospitalized. Patient recovered.

Neupro Side Effects Report #5788176-5
NEUPRO problem was reported by a Physician from UNITED STATES on June 05, 2008. Female patient was diagnosed with parkinson's disease and was treated with NEUPRO. After drug was administered, patient experienced the following problems/side effects: decreased activity, ill-defined disorder, impaired driving ability, . NEUPRO dosage: 6MG/24H, 1 IN 1 D, TRANSDERMAL. Patient recovered.

Zyprexa Side Effects Report #5730045-0
Consumer or non-health professional from UNITED STATES reported ZYPREXA problem on Apr 28, 2008. Female patient was diagnosed with schizophrenia and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: decreased activity, depressed level of consciousness, feeling of despair, hypernatraemia, marital problem, overdose, social avoidant behaviour, suicide attempt, white blood cell count increased, . ZYPREXA dosage: 20 MG, UNK. During the same period patient was treated with ZOLOFT. Patient was hospitalized. Patient recovered.

Digoxin Side Effects Report #5736211-2
DIGOXIN problem was reported by a Pharmacist from UNITED STATES on May 09, 2008. Female patient, 83 years of age, was diagnosed with cardiac disorder and was treated with DIGOXIN. After drug was administered, patient experienced the following problems/side effects: decreased activity, dyspnoea, fatigue, . DIGOXIN dosage: unknown. Patient recovered.

Digoxin Side Effects Report #5742211-9
Consumer or non-health professional from UNITED STATES reported DIGOXIN problem on May 14, 2008. Male patient, 36 years of age, weighting 190.0 lb, was diagnosed with cardiomyopathy and was treated with DIGOXIN. After drug was administered, patient experienced the following problems/side effects: decreased activity, fatigue, feeling abnormal, listless, nausea, overdose, vomiting, . DIGOXIN dosage: unknown. Patient recovered.

Rozerem Side Effects Report #5745480-4
ROZEREM problem was reported by a Health Professional from UNITED STATES on Apr 16, 2008. Female patient, 52 years of age, weighting 189.0 lb, was diagnosed with insomnia and was treated with ROZEREM. After drug was administered, patient experienced the following problems/side effects: decreased activity, eating disorder, major depression, overdose, poor quality sleep, . ROZEREM dosage: 8 MG, QHS, PER ORAL ; 1-2 TABLETS, 8 MG, QHS, PER ORAL. During the same period patient was treated with KLONOPIN, WELLBUTRIN, TRAZODONE, TOPAMAX. Patient recovered.

Vesicare Side Effects Report #5749097-7
Physician from JAPAN reported VESICARE problem on May 15, 2008. Female patient, weighting 57.32 lb, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: decreased activity, decreased appetite, marasmus, renal impairment, . VESICARE dosage: 5 MG, UID/QD, ORAL. During the same period patient was treated with NORVASC, LISINOPRIL. Patient died on 01/25/2008.

Rozerem Side Effects Report #5671978-3
ROZEREM problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 15, 2007. Male patient, 57 years of age, weighting 237.0 lb, was diagnosed with middle insomnia and was treated with ROZEREM. After drug was administered, patient experienced the following problems/side effects: decreased activity, hangover, middle insomnia, . ROZEREM dosage: 8 MG, QHS, PER ORAL. During the same period patient was treated with PREVACID. Patient recovered.

Rozerem Side Effects Report #5672769-X
Consumer or non-health professional from UNITED STATES reported ROZEREM problem on Jan 21, 2008. Female patient, 75 years of age, weighting 110.0 lb, was diagnosed with insomnia and was treated with ROZEREM. After drug was administered, patient experienced the following problems/side effects: decreased activity, feeling jittery, initial insomnia, somnolence, . ROZEREM dosage: 8 MG, QHS PRN, PER ORAL. During the same period patient was treated with SYNTHROID, COZAAR, ASPIRIN, VITAMINS, ALPHAGAN. Patient recovered.

Comtan Side Effects Report #5697443-5
COMTAN problem was reported by a Physician from JAPAN on Apr 01, 2008. Female patient, 74 years of age, was diagnosed with parkinson's disease, oedema, hyperlipidaemia and was treated with COMTAN. After drug was administered, patient experienced the following problems/side effects: decreased activity, fall, gait disturbance, . COMTAN dosage: 400 MG/DAY. During the same period patient was treated with CARBIDOPA AND LEVODOPA, CABERGOLINE, DOMIN, SELEGILINE, ALDACTONE, MEVALOTIN. Patient was hospitalized. Patient recovered.

Comtan Side Effects Report #5711710-8
Physician from JAPAN reported COMTAN problem on Apr 15, 2008. Female patient, 74 years of age, was diagnosed with parkinson's disease, oedema, hyperlipidaemia and was treated with COMTAN. After drug was administered, patient experienced the following problems/side effects: decreased activity, fall, gait disturbance, . COMTAN dosage: 400 MG/DAY. During the same period patient was treated with MENESIT, CABASER, DOMIN, SELEGILINE, ALDACTONE, MEVALOTIN. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5319547-9
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 27, 2007. Female patient was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: decreased activity, endometrial cancer, endometrial hyperplasia, lymphadenectomy, uterine polyp, . FORTEO dosage: unknown. Patient recovered.

Topamax Side Effects Report #5327821-5
Physician from GERMANY reported TOPAMAX problem on May 08, 2007. Female patient, 42 years of age, was diagnosed with epilepsy and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: decreased activity, mental disorder, motor dysfunction, pseudodementia, . TOPAMAX dosage: unknown. Patient recovered.

Valtrex Side Effects Report #5283202-4
VALTREX problem was reported by a Physician from JAPAN on Mar 29, 2007. Male patient, 87 years of age, weighting 132.3 lb, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: decreased activity, dehydration, depressed level of consciousness, dizziness, dysarthria, dyslalia, nervous system disorder, pain, renal failure, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with LOXONIN, SELBEX, MUCOSTA, ALLOZYM, NORVASC, ANPLAG, KERLONG, PRERAN. Patient was hospitalized and became disabled. Patient recovered.

Lanoxin Side Effects Report #5299914-2
Consumer or non-health professional from UNITED KINGDOM reported LANOXIN problem on Mar 28, 2007. Male patient, 68 years of age, weighting 171.6 lb, was treated with LANOXIN. After drug was administered, patient experienced the following problems/side effects: decreased activity, dissociation, dizziness, dyspnoea, fatigue, oedema, paraesthesia, ventricular dysfunction, . LANOXIN dosage: .125 MG PER DAY. During the same period patient was treated with FUROSEMIDE, ASPIRIN, AMIODARONE, EZETIMIBE, LANSOPRAZOLE. Patient recovered.

Penicillin Side Effects Report #5311887-2
PENICILLIN G problem was reported by a Physician from UNITED STATES on Apr 26, 2007. Female patient, 38 years of age, weighting 120.0 lb, was diagnosed with animal bite and was treated with PENICILLIN G. After drug was administered, patient experienced the following problems/side effects: decreased activity, infusion site bruising, injection site phlebitis, pain, . PENICILLIN G dosage: I THINK 2 MILLION UNITS Q4 IV DRIP. During the same period patient was treated with OXYCODONE, ZOFRAN. Patient recovered.

Cymbalta Side Effects Report #5340023-1
Consumer or non-health professional from UNITED STATES reported CYMBALTA problem on Nov 16, 2006. Male patient was diagnosed with back pain and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: decreased activity, dizziness, feeling abnormal, tinnitus, . CYMBALTA dosage: unknown. During the same period patient was treated with OXYCONTIN, CELEBREX. Patient recovered.

Cymbalta Side Effects Report #5340954-2
CYMBALTA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2006. Female patient, 55 years of age, was diagnosed with depression and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: decreased activity, fatigue, . CYMBALTA dosage: unknown. During the same period patient was treated with WELLBUTRIN, PREVACID, VALTREX. Patient recovered.

Requip Side Effects Report #5257994-4
Consumer or non-health professional from UNITED STATES reported REQUIP problem on Nov 28, 2006. Female patient was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: decreased activity, disability, malaise, . REQUIP dosage: 1MG PER DAY. Patient recovered.

Valtrex Side Effects Report #5264838-3
VALTREX problem was reported by a Physician from JAPAN on Mar 06, 2007. Male patient, 87 years of age, weighting 132.3 lb, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: decreased activity, dehydration, depressed level of consciousness, dizziness, dysarthria, dyslalia, eating disorder, pain, . VALTREX dosage: 1000MG THREE TIMES PER DAY. During the same period patient was treated with LOXONIN, SELBEX, MUCOSTA, ALLOZYM, NORVASC, ANPLAG, KERLONG, PRERAN. Patient was hospitalized and became disabled. Patient recovered.

Bextra Side Effects Report #5271251-1
Physician from UNITED STATES reported BEXTRA problem on July 15, 2006. Female patient, 69 years of age, was diagnosed with nerve injury, pain and was treated with BEXTRA. After drug was administered, patient experienced the following problems/side effects: decreased activity, depression, nausea, obesity, . BEXTRA dosage: unknown. During the same period patient was treated with CELEBREX, DARVOCET, CHLORTHALIDONE, PAXIL. Patient recovered.

Rebif Side Effects Report #5277571-9
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 31, 2007. Female patient, 26 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: decreased activity, multiple sclerosis, pain, parvovirus infection, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5656254-7
Physician from JAPAN reported VELCADE problem on Feb 21, 2008. Male patient was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: anorexia, decreased activity, malaise, pancytopenia, sepsis, . VELCADE dosage: 1.30 MG/M2, INTRAVENOUS. Patient recovered.

Chantix Side Effects Report #5662199-9
CHANTIX problem was reported by a Health Professional from UNITED KINGDOM on Mar 04, 2008. Female patient, 59 years of age, weighting 140.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: aggression, decreased activity, insomnia, panic attack, paranoia, somnolence, . CHANTIX dosage: unknown. Patient recovered.

Revatio Side Effects Report #5676386-7
Consumer or non-health professional from UNITED STATES reported REVATIO problem on Mar 11, 2008. Male patient, weighting 185.0 lb, was diagnosed with pulmonary hypertension and was treated with REVATIO. After drug was administered, patient experienced the following problems/side effects: cough, decreased activity, pain in extremity, paraesthesia, sinus headache, . REVATIO dosage: unknown. During the same period patient was treated with WARFARIN, NONSELECTIVE ENDOTHELIN RECEPTOR ANTAGONIST. Patient recovered.