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

HYPOTENSION ( 9 FDA reports)
PYREXIA ( 6 FDA reports)
DYSPNOEA ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ( 5 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
FALL ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
APATHY ( 1 FDA reports)
APLASIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CNS VENTRICULITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICROCOCCUS INFECTION ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHYTHM IDIOVENTRICULAR ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENOSYNOVITIS ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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