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

PYREXIA ( 37 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 24 FDA reports)
NEUTROPENIA ( 24 FDA reports)
RENAL FAILURE ( 22 FDA reports)
CHOLESTASIS ( 18 FDA reports)
ANAEMIA ( 16 FDA reports)
CONVULSION ( 15 FDA reports)
SUBDURAL HAEMATOMA ( 15 FDA reports)
FALL ( 14 FDA reports)
ARTHRALGIA ( 11 FDA reports)
ABSCESS ( 9 FDA reports)
AGRANULOCYTOSIS ( 9 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 9 FDA reports)
LARGE INTESTINE PERFORATION ( 9 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
PANCREATITIS ( 8 FDA reports)
INFECTION ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
PAIN ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
FANCONI SYNDROME ACQUIRED ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
ANAEMIA NEONATAL ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 4 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COMA ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MICROTIA ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYCOBACTERIA BLOOD TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUBERCULOSIS LIVER ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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