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

PREGNANCY ( 17 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
CONVULSION ( 5 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 4 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
MANIA ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER CANCER RECURRENT ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
VESTIBULAR DISORDER ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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