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

BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
FALL ( 5 FDA reports)
ALCOHOL USE ( 4 FDA reports)
COMA ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
MELAENA ( 3 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CHEST WALL PAIN ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS PSORIASIFORM ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS C VIRUS TEST POSITIVE ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERKERATOSIS PALMARIS AND PLANTARIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MENINGORRHAGIA ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
OESTRADIOL INCREASED ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STRESS CARDIOMYOPATHY ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BLOOD FOLATE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COXIELLA INFECTION ( 1 FDA reports)
CRYOGLOBULINS PRESENT ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
FOETAL MACROSOMIA ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MEASLES ANTIBODY POSITIVE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
ZIEVE SYNDROME ( 1 FDA reports)

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