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

DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
COMPULSIVE SHOPPING ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
POTTER'S SYNDROME ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
ASTHENIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
AMIMIA ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
ACALCULIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE THROMBOSIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC BEHAVIOUR ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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