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

NEUROPATHY PERIPHERAL ( 24 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
NAUSEA ( 6 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
HEMIVERTEBRA ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
OESOPHAGEAL ATRESIA ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
AGGRESSION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACNE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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