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

DYSPNOEA ( 14 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
NASAL CONGESTION ( 7 FDA reports)
BRONCHIAL OBSTRUCTION ( 6 FDA reports)
ANORGASMIA ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
EJACULATION FAILURE ( 4 FDA reports)
URTICARIA ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
RASH ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
FALL ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PEYRONIE'S DISEASE ( 2 FDA reports)
INJURY ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)

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