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

BLOOD PRESSURE DECREASED ( 9 FDA reports)
LIVER DISORDER ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
SWELLING FACE ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ANAEMIA POSTOPERATIVE ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OPERATIVE HAEMORRHAGE ( 4 FDA reports)
PROCEDURAL HYPOTENSION ( 4 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
THREATENED LABOUR ( 3 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL STONE REMOVAL ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMA ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)

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