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

DRUG INTERACTION ( 6 FDA reports)
DIZZINESS ( 4 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
GALACTORRHOEA ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELIRIUM ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
FALL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SOPOR ( 1 FDA reports)
AGITATION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)

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