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

CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
HYPERTENSION ( 3 FDA reports)
HAEMANGIOMA OF SKIN ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
RETROPERITONEAL FIBROSIS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
POLYCHONDRITIS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
DEAFNESS CONGENITAL ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
TENDON SHEATH INCISION ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EPISTAXIS ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
DEATH ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHANGIOMA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)

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