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

DRUG INTERACTION ( 16 FDA reports)
AGRANULOCYTOSIS ( 10 FDA reports)
RASH ( 9 FDA reports)
PNEUMONIA ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
SALIVARY GLAND CALCULUS ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
AGITATION ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
LARGE INTESTINE PERFORATION ( 4 FDA reports)
MELAENA ( 4 FDA reports)
POST PROCEDURAL URINE LEAK ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANGIOPLASTY ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
EPICONDYLITIS ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
ILEUS ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
VASCULAR ENCEPHALOPATHY ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TRACHEAL DISORDER ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BONE DENSITOMETRY ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
CAMPTOCORMIA ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COMA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS HELICOBACTER ( 1 FDA reports)
GENERAL ANAESTHESIA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUMBAR VERTEBRA INJURY ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL MUCOSAL DISORDER ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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