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

PLATELET COUNT DECREASED ( 21 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 15 FDA reports)
CARDIAC FAILURE ( 13 FDA reports)
LIVER DISORDER ( 13 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
CARDIAC AMYLOIDOSIS ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
CHEYNE-STOKES RESPIRATION ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
VOMITING ( 9 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 8 FDA reports)
ATRIAL FLUTTER ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
NAUSEA ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
FRACTURE ( 5 FDA reports)
HEPATITIS B ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
MALAISE ( 5 FDA reports)
NEPHRITIS INTERSTITIAL ( 5 FDA reports)
PAIN ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
ASPHYXIA ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DEATH ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSEUDO-BARTTER SYNDROME ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)

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