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

DEHYDRATION ( 22 FDA reports)
RENAL FAILURE ACUTE ( 21 FDA reports)
VOMITING ( 19 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 17 FDA reports)
MALAISE ( 14 FDA reports)
NAUSEA ( 13 FDA reports)
PYREXIA ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
BLOOD UREA INCREASED ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
PLATELET COUNT DECREASED ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
MENIERE'S DISEASE ( 7 FDA reports)
METASTASES TO BONE ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
TINNITUS ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
BASAL CELL CARCINOMA ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
AUTOPHONY ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
ILEUS ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
PAIN ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PRESBYACUSIS ( 4 FDA reports)
RASH ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DYSLALIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERCHLORAEMIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
TINEA PEDIS ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DEAFNESS TRANSITORY ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPH NODE PALPABLE ( 2 FDA reports)
MALIGNANT CRANIAL NERVE NEOPLASM ( 2 FDA reports)
MERALGIA PARAESTHETICA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ARTHRITIS GONOCOCCAL ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HEAT EXHAUSTION ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MANIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SHOCK ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRESS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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