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

CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
DEPRESSION ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
TREMOR ( 4 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PAIN ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ATROPHIC VULVOVAGINITIS ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
GRANDIOSITY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEREDITARY ANGIOEDEMA ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VOMITING ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FOLATE ABNORMAL ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FALL ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
TESTICULAR OEDEMA ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 ABNORMAL ( 1 FDA reports)

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