ADVERSE EVENT side effect
What is ADVERSE EVENT ?Drugs associated with ADVERSE EVENT
ABRAXANE ADVAIR ALBUMINAR ALBUTEROL ALEVE ALTABAX AMOXICILLIN ARIMIDEX ARIXTRA AUGMENTIN AVANDAMET AVANDARYL AVANDIA AVAPRO AVELOX AVODART BACLOFEN BONIVA BUPROPION BYETTA CADUET CASODEX CHANTIX CIALIS CIPRO CITALOPRAM CLAVAMOX COMBIVIR COMMIT COREG DASATINIB DECADRON DEFINITY DETROL DILANTIN DURAGESIC EFFEXOR EMSAM ENBREL ERBITUX EXENATIDE EYE FABRAZYME FASTIN FLONASE FLOVENT FOSAMAX GLUCOPHAGE GOODYS HALDOL HEPARIN HERCEPTIN HUMIRA HYCAMTIN IBUPROFEN IMITREX INFLIXIMAB INVEGA IRINOTECAN ISOPTIN JANUMET JANUVIA KENACORT LAMICTAL LEUKINE LEVITRA LIPITOR LYRICA MAGNEVIST MALARONE MAXALT MAXIPIME MEGACE MERIDIA MICARDIS MINIMS MIRENA MODURETIC NEULASTIM NEUROLITE NEURONTIN NICODERM NICORETTE NIFEDIPINE ORENCIA PAROXETINE PAXIL PEGASYS PRIALT PRILOSEC PRIMAXIN PROCRIT PROPECIA PROSCAR PROVIGIL REBIF REMICADE REQUIP REVLIMID RISPERDAL ROZEREM SERETIDE SEROQUEL SEROXAT SERZONE SIMVASTATIN SINGULAIR SORAFENIB SPRYCEL SUTENT TARCEVA TAXOL TRASYLOL TRICOR TRIZIVIR TYKERB TYSABRI ULTRAVIST VALACYCLOVIR VALTREX VANCOMYCIN VENTOLIN VERAMYST VFEND VIAGRA VYTORIN VYVANSE WELLBUTRIN XOLAIR ZANTAC ZETIA ZIAGEN ZOCOR ZOLINZA ZYFLOADVERSE EVENT : Micardis Side Effects Report #5647846-X
Consumer or non-health professional from JAPAN reported MICARDIS problem on Feb 26, 2008. Female patient, weighting 158.7 lb, was diagnosed with hypertension and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: adverse event, . MICARDIS dosage: unknown. During the same period patient was treated with INSULIN. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Magnevist Side Effects Report #5648996-4
MAGNEVIST problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 01, 2008. Female patient, 50 years of age, was diagnosed with nuclear magnetic resonance imaging and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: adverse event, . MAGNEVIST dosage: unknown. Patient recovered.
ADVERSE EVENT : Bupropion Side Effects Report #5651046-7
Consumer or non-health professional from UNITED STATES reported BUPROPION HYDROCHLORIDE problem on Feb 26, 2008. Female patient was diagnosed with depression and was treated with BUPROPION HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: adverse event, aggression, . BUPROPION HYDROCHLORIDE dosage: 300MGD PER DAY. Patient recovered.
ADVERSE EVENT : Requip Side Effects Report #5653398-0
REQUIP problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2008. Male patient, 54 years of age, was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: adverse event, alcohol use, feeling abnormal, gambling, mania, nicotine dependence, obsessive-compulsive disorder, personality change, theft, . REQUIP dosage: 2MG PER DAY. During the same period patient was treated with NEURONTIN, LEXAPRO, CLONAZEPAM. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Requip Side Effects Report #5655053-X
Consumer or non-health professional from UNITED STATES reported REQUIP problem on Nov 26, 2007. Female patient was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: adverse event, joint swelling, sleep disorder, . REQUIP dosage: 1.5MG SEE TEXT. Patient recovered.
ADVERSE EVENT : Malarone Side Effects Report #5655246-1
MALARONE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 27, 2008. Female patient, 27 years of age, was diagnosed with malaria prophylaxis and was treated with MALARONE. After drug was administered, patient experienced the following problems/side effects: adverse event, delusion, fear, hallucination, hypertension, insomnia, palpitations, . MALARONE dosage: unknown. During the same period patient was treated with BIRTH CONTROL. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5655384-3
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Feb 28, 2008. Female patient, 84 years of age, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, . FOSAMAX dosage: unknown. Patient died on 05/28/2006.
ADVERSE EVENT : Fosamax Side Effects Report #5655411-3
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 27, 2008. Female patient, 60 years of age, weighting 191.8 lb, was diagnosed with osteopenia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, anxiety, depression, inflammatory bowel disease, osteonecrosis, tooth loss, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.
ADVERSE EVENT : Vytorin Side Effects Report #5657160-4
Physician from GERMANY reported VYTORIN problem on Feb 29, 2008. Male patient, 57 years of age, weighting 220.5 lb, was diagnosed with type iia hyperlipidaemia and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: adverse event, colon adenoma, diarrhoea haemorrhagic, influenza like illness, intestinal polyp, pneumonia, renal failure acute, rhabdomyolysis, . VYTORIN dosage: unknown. During the same period patient was treated with ASPIRIN. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5657162-8
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Feb 26, 2008. Female patient, 63 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, angiopathy, depression, infection, pancytopenia, resorption bone increased, tooth fracture, . FOSAMAX dosage: unknown. During the same period patient was treated with FOSAMAX PLUS D. Patient was hospitalized and became disabled. Patient recovered.
ADVERSE EVENT : Heparin Side Effects Report #5657323-8
Consumer or non-health professional from UNITED STATES reported HEPARIN problem on Mar 03, 2008. Female patient, 92 years of age, was diagnosed with stent placement and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: adverse event, atrial fibrillation, blood pressure decreased, loss of consciousness, pruritus, swollen tongue, . HEPARIN dosage: unknown. During the same period patient was treated with PLAVIX, COREG, BENICAR, NORVASC, OMEGA, SYNTHROID, NITROGLYCERIN. Patient recovered.
ADVERSE EVENT : Aleve Side Effects Report #5659276-5
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on July 27, 2007. Female patient, 55 years of age, weighting 149.9 lb, was diagnosed with back pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: adverse event, dysgeusia, stomach discomfort, . ALEVE dosage: TOTAL DAILY DOSE: 440 MG UNIT DOSE: 220 MG. During the same period patient was treated with THYROID. Patient recovered.
ADVERSE EVENT : Invega Side Effects Report #5660724-5
Physician from CANADA reported INVEGA problem on Mar 07, 2008. Male patient, 17 years of age, was treated with INVEGA. After drug was administered, patient experienced the following problems/side effects: adverse event, . INVEGA dosage: unknown. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Zolinza Side Effects Report #5661463-7
ZOLINZA problem was reported by a Pharmacist from UNITED STATES on Mar 10, 2008. Male patient, 15 years of age, was diagnosed with t-cell lymphoma and was treated with ZOLINZA. After drug was administered, patient experienced the following problems/side effects: adverse event, neuropathy peripheral, t-cell lymphoma recurrent, . ZOLINZA dosage: unknown. During the same period patient was treated with ALEMTUZUMAB, BORTEZOMIB, MEPERIDINE HYDROCHLORIDE, BACTRIM, VORICONAZOLE, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Kenacort Side Effects Report #5661669-7
Physician from BELGIUM reported KENACORT problem on Mar 11, 2008. Female patient, 57 years of age, weighting 132.3 lb, was diagnosed with carpal tunnel syndrome and was treated with KENACORT. After drug was administered, patient experienced the following problems/side effects: adverse event, . KENACORT dosage: unknown. Patient recovered.
ADVERSE EVENT : Micardis Side Effects Report #5662111-2
MICARDIS problem was reported by a Physician from JAPAN on Mar 06, 2008. Female patient, weighting 167.6 lb, was diagnosed with hypertension and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: adverse event, . MICARDIS dosage: unknown. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Vytorin Side Effects Report #5662278-6
Physician from GERMANY reported VYTORIN problem on Mar 10, 2008. Male patient, 57 years of age, weighting 220.5 lb, was diagnosed with type iia hyperlipidaemia and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: adverse event, colon adenoma, diarrhoea haemorrhagic, haematuria, influenza like illness, intestinal polyp, pneumonia, renal failure acute, rhabdomyolysis, . VYTORIN dosage: unknown. During the same period patient was treated with ASPIRIN. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5662936-3
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 28, 2008. Female patient, 64 years of age, weighting 160.9 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, anxiety, blood cholesterol increased, blood pressure increased, bronchitis, cellulitis, cerebrovascular accident, cerebrovascular disorder, chest pain, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Zetia Side Effects Report #5663538-5
Pharmacist from CANADA reported ZETIA problem on Mar 10, 2008. Female patient, 59 years of age, was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: adverse event, hepatic enzyme increased, . ZETIA dosage: unknown. During the same period patient was treated with ZOCOR. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Paxil Side Effects Report #5664470-3
PAXIL problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 06, 2008. Male patient, 35 years of age, was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: adverse event, depressed level of consciousness, headache, homicide, laboratory test abnormal, loss of consciousness, withdrawal syndrome, . PAXIL dosage: unknown. During the same period patient was treated with DOXEPIN, RITALIN, PROVIGIL, TESTOSTERONE. Patient recovered.
ADVERSE EVENT : Propecia Side Effects Report #5665148-2
Physician from UNITED KINGDOM reported PROPECIA problem on Mar 05, 2008. Female patient, 35 years of age, was treated with PROPECIA. After drug was administered, patient experienced the following problems/side effects: adverse event, umbilical hernia, . PROPECIA dosage: unknown. During the same period patient was treated with DIBUCAINE HYDROCHLORIDE AND PREDNISOLONE HEXANOATE, FERROUS SULPHATE, DIBUCAINE HYDROCHLORIDE AND PREDNISOLONE HEXANOATE, ACETAMINOPHEN, AMOXICILLIN, CALCIUM CARBONATE AND ALGINATE AND BICARBONATE, ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5669373-6
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 06, 2008. Female patient, 66 years of age, weighting 136.7 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, anaemia, bipolar i disorder, bone pain, cervical cord compression, constipation, contusion, deep vein thrombosis, facial pain, . FOSAMAX dosage: unknown. During the same period patient was treated with ACTONEL. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Lamictal Side Effects Report #5669410-9
Consumer or non-health professional from UNITED STATES reported LAMICTAL problem on Mar 07, 2008. Female patient, 38 years of age, was diagnosed with bipolar disorder, alopecia and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: adverse event, bacterial infection, blister, chest pain, coma, conjunctivitis, dysphagia, dyspnoea, . LAMICTAL dosage: unknown. During the same period patient was treated with CLONAZEPAM, BENZTROPINE MESYLATE, FLOVENT, ALBUTEROL. Patient was hospitalized and became disabled. Patient recovered.
ADVERSE EVENT : Requip Side Effects Report #5669415-8
REQUIP problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 06, 2008. Male patient, 54 years of age, was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: adverse event, alcohol use, feeling abnormal, gambling, mania, nicotine dependence, obsessive-compulsive disorder, personality change, theft, . REQUIP dosage: 2MG PER DAY. During the same period patient was treated with NEURONTIN, LEXAPRO, CLONAZEPAM. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5670059-2
Consumer or non-health professional from AUSTRALIA reported FOSAMAX problem on Mar 10, 2008. Female patient, 77 years of age, was diagnosed with osteoporosis, hypertension, rheumatoid arthritis, prophylaxis against gastrointestinal ulcer and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, bradycardia, circulatory collapse, malaise, thrombosis, . FOSAMAX dosage: unknown. During the same period patient was treated with LISINOPRIL, AMLODIPINE BESYLATE, ALLOPURINOL, OMEPRAZOLE MAGNESIUM. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5670856-3
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Mar 07, 2008. Male patient, 51 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, breath odour, carpal tunnel syndrome, loose tooth, rheumatoid arthritis, . FOSAMAX dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient was hospitalized and became disabled. Patient recovered.
ADVERSE EVENT : Risperdal Side Effects Report #5670986-6
Consumer or non-health professional from UNITED STATES reported RISPERDAL problem on Mar 10, 2008. Male patient, weighting 171.0 lb, was diagnosed with tic, tourette's disorder and was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: adverse event, agitation, anxiety, blood triglycerides increased, chest pain, diabetes mellitus, dysphagia, epiglottitis, . RISPERDAL dosage: unknown. During the same period patient was treated with SEROQUEL, TOPROL, KLONOPIN, NITRO. Patient recovered.
ADVERSE EVENT : Moduretic Side Effects Report #5671567-0
MODURETIC problem was reported by a Physician from AUSTRIA on Mar 12, 2008. Female patient, 92 years of age, was diagnosed with hypertension and was treated with MODURETIC. After drug was administered, patient experienced the following problems/side effects: adverse event, blood electrolytes decreased, syncope, . MODURETIC dosage: unknown. During the same period patient was treated with HYDROCHLOROTHIAZIDE AND LOSARTAN POTASSIUM. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5672623-3
Physician from UNITED STATES reported FOSAMAX problem on Mar 11, 2008. Female patient, 64 years of age, weighting 160.9 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, anxiety, blood cholesterol increased, blood pressure increased, bronchitis, cellulitis, cerebrovascular accident, cerebrovascular disorder, chest pain, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Fabrazyme Side Effects Report #5673021-9
FABRAZYME problem was reported by a Physician from AUSTRALIA on Mar 03, 2008. Male patient, 40 years of age, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: adverse event, anxiety, chest discomfort, dialysis, disease recurrence, feeling abnormal, renal failure, . FABRAZYME dosage: 75 MG, INTRAVENOUS. Patient recovered.
ADVERSE EVENT : Fabrazyme Side Effects Report #5673052-9
Physician from AUSTRALIA reported FABRAZYME problem on Mar 03, 2008. Male patient, 40 years of age, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: adverse event, anxiety, chest discomfort, feeling abnormal, renal failure, . FABRAZYME dosage: 75 MG, INTRAVENOUS. Patient recovered.
ADVERSE EVENT : Lamictal Side Effects Report #5674645-5
LAMICTAL problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 14, 2008. Female patient, 38 years of age, was diagnosed with bipolar disorder and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: adverse event, bacterial infection, blister, chest pain, coma, conjunctivitis, dysphagia, dyspnoea, . LAMICTAL dosage: 50MG PER DAY. During the same period patient was treated with CLONAZEPAM, BENZTROPINE MESYLATE, FLOVENT, ALBUTEROL, HYDROXYZINE. Patient was hospitalized and became disabled. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5675408-7
Health Professional from UNITED STATES reported FOSAMAX problem on Mar 12, 2008. Female patient, 65 years of age, weighting 99.21 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, candidiasis, cryoglobulinaemia, depression, epistaxis, glossitis, hepatitis c, insomnia, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Heparin Side Effects Report #5675649-9
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 14, 2008. Female patient, 52 years of age, was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: adverse event, . HEPARIN dosage: unknown. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Valtrex Side Effects Report #5675893-0
Consumer or non-health professional from UNITED STATES reported VALTREX problem on Mar 17, 2008. Female patient, 64 years of age, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: adverse event, aphasia, convulsion, depression, dysstasia, hallucination, overdose, speech disorder, . VALTREX dosage: 1000MG TWICE PER DAY. During the same period patient was treated with INSULIN, RENAGEL, COZAAR, NORVASC, LEVOTHYROXINE, ZOFRAN, ANTIBIOTICS, CHLORIDE. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5676882-2
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 13, 2008. Female patient, 66 years of age, weighting 136.7 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, bipolar i disorder, bone pain, cervical cord compression, constipation, contusion, deep vein thrombosis, facial pain, fall, . FOSAMAX dosage: unknown. During the same period patient was treated with ACTONEL. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Requip Side Effects Report #5677152-9
Consumer or non-health professional from UNITED STATES reported REQUIP problem on Mar 13, 2008. Male patient, 54 years of age, was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: adverse event, alcohol use, alcoholism, confabulation, feeling abnormal, gambling, mania, nicotine dependence, obsessive-compulsive disorder, . REQUIP dosage: 2MG PER DAY. During the same period patient was treated with NEURONTIN, LEXAPRO, CLONAZEPAM. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Neulastim Side Effects Report #5678561-4
NEULASTIM problem was reported by a Physician from ISRAEL on Mar 11, 2008. Male patient, 50 years of age, was treated with NEULASTIM. After drug was administered, patient experienced the following problems/side effects: adverse event, confusional state, convulsion, dizziness, leukocytosis, nausea, syncope, vomiting, . NEULASTIM dosage: unknown. During the same period patient was treated with ETOPOSIDE, CISPLATIN, CARBOPLATIN, ATENOLOL, ASPIRIN, ATORVASTATIN CALCIUM, LANSOPRAZOLE, OXYCONTIN. Patient was hospitalized. Patient died on 01/09/2008.
ADVERSE EVENT : Requip Side Effects Report #5678991-0
Physician from UNITED STATES reported REQUIP problem on Mar 24, 2008. Male patient, 54 years of age, was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: adverse event, alcohol use, alcoholism, bipolar disorder, confabulation, feeling abnormal, gambling, impaired self-care, mania, . REQUIP dosage: 2MG PER DAY. During the same period patient was treated with NEURONTIN, LEXAPRO, CLONAZEPAM. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Chantix Side Effects Report #5679425-2
CHANTIX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 13, 2008. Female patient, weighting 140.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: adverse event, anuria, cystitis, weight increased, . CHANTIX dosage: unknown. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5680540-8
Physician from UNITED STATES reported FOSAMAX problem on Mar 19, 2008. Female patient, 61 years of age, weighting 160.9 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, anxiety, blood cholesterol increased, blood pressure increased, bronchitis, cellulitis, cerebrovascular accident, cerebrovascular disorder, chest pain, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5682962-8
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 18, 2008. Female patient, 84 years of age, weighting 143.3 lb, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, anaemia, blood creatinine increased, breath sounds abnormal, cardiac failure, dyspnoea, eosinophilia, hyponatraemia, myocardial infarction, . FOSAMAX dosage: unknown. During the same period patient was treated with LASIX, DIOVAN, HYDROCORTISONE OINTMENT, NITROGLYCERIN, PREVACID, FOLIC ACID, FERROUS SULPHATE, RENAGEL. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Fosamax Side Effects Report #5684452-5
Physician from UNITED STATES reported FOSAMAX problem on Mar 19, 2008. Female patient, 35 years of age, weighting 216.1 lb, was diagnosed with osteoporosis, osteopenia, convulsion, pain, prophylaxis of nausea and vomiting, motion sickness and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: adverse event, ankle fracture, anxiety, cervix carcinoma, deafness, depression, foot fracture, injury, jaw disorder, . FOSAMAX dosage: unknown. During the same period patient was treated with TOPAMAX, NEURONTIN, VICODIN, PROMETHAZINE. Patient was hospitalized and became disabled. Patient recovered.
ADVERSE EVENT : Vytorin Side Effects Report #5684453-7
VYTORIN problem was reported by a Pharmacist from UNITED STATES on Mar 24, 2008. Male patient, 57 years of age, was diagnosed with hypercholesterolaemia and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: adverse event, anxiety, depression, emotional disorder, . VYTORIN dosage: unknown. During the same period patient was treated with EFFEXOR, ARICEPT, CLONAZEPAM. Patient recovered.
ADVERSE EVENT : Erbitux Side Effects Report #5684938-3
Consumer or non-health professional from UNITED STATES reported ERBITUX problem on Jan 10, 2008. Male patient, 86 years of age, weighting 224.9 lb, was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: adverse event, . ERBITUX dosage: unknown. Patient was hospitalized. Patient recovered.
ADVERSE EVENT : Mirena Side Effects Report #5685880-4
MIRENA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 01, 2007. Female patient was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: adverse event, . MIRENA dosage: unknown. Patient recovered.
ADVERSE EVENT : Mirena Side Effects Report #5685881-6
Health Professional from UNITED STATES reported MIRENA problem on Aug 30, 2007. Female patient was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: adverse event, . MIRENA dosage: unknown. Patient recovered.
ADVERSE EVENT : Levitra Side Effects Report #5685908-1
LEVITRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2008. Male patient was treated with LEVITRA. After drug was administered, patient experienced the following problems/side effects: adverse event, . LEVITRA dosage: unknown. Patient recovered.
ADVERSE EVENT : Mirena Side Effects Report #5685973-1
Consumer or non-health professional from UNITED STATES reported MIRENA problem on Sept 11, 2007. Female patient, 39 years of age, weighting 196.2 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: adverse event, intra-uterine contraceptive device expelled, vaginal haemorrhage, . MIRENA dosage: unknown. Patient recovered.
ADVERSE EVENT : Mirena Side Effects Report #5686442-5
MIRENA problem was reported by a Consumer or non-health professional from UNITED STATES on July 25, 2007. Female patient was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: adverse event, . MIRENA dosage: unknown. Patient recovered.
ADVERSE EVENT : Mirena Side Effects Report #5686664-3
Physician from UNITED STATES reported MIRENA problem on May 22, 2007. Female patient was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: adverse event, . MIRENA dosage: unknown. Patient recovered.