Please choose an event type to view the corresponding MedsFacts report:

HOT FLUSH ( 7 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
DEPRESSION ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
CRYING ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
ANGER ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
FALL ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
ATROPHIC VULVOVAGINITIS ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONIC OBSTRUCTION ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)

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