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

DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
TRISOMY 21 ( 7 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 6 FDA reports)
SKIN EXFOLIATION ( 6 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 6 FDA reports)
PYREXIA ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
CHEILITIS ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
FALLOT'S TETRALOGY ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
VULVAL DISORDER ( 4 FDA reports)
VULVITIS ( 4 FDA reports)
DELIRIUM ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
UMBILICAL ERYTHEMA ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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