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

CYTOLYTIC HEPATITIS ( 12 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
CHOLESTASIS ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
DEATH ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
SUBDURAL HAEMATOMA ( 5 FDA reports)
TONGUE OEDEMA ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
FALL ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ANAEMIA MACROCYTIC ( 3 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ANURIA ( 3 FDA reports)
APOPTOSIS ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE ABNORMAL ( 3 FDA reports)
CHLAMYDIA TEST POSITIVE ( 3 FDA reports)
COMA ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EMPHYSEMA ( 3 FDA reports)
ENANTHEMA ( 3 FDA reports)
EPIDERMAL NECROSIS ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENITAL EROSION ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
OPTIC NERVE CUPPING ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PO2 INCREASED ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RASH ( 3 FDA reports)
SCROTAL ULCER ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
VITAMIN B12 INCREASED ( 3 FDA reports)
VOCAL CORD INFLAMMATION ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AORTIC CALCIFICATION ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHOREA ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS ALCOHOLIC ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SCAR ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SURGERY ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENSION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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