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

ABORTION SPONTANEOUS ( 15 FDA reports)
STILLBIRTH ( 8 FDA reports)
DEHYDRATION ( 5 FDA reports)
PEPTIC ULCER ( 5 FDA reports)
DIARRHOEA ( 4 FDA reports)
DEATH ( 4 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
PULMONARY VALVE STENOSIS ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 3 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ASTHENIA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
COUGH ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
DELIRIUM ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
PALLOR ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE ABNORMAL ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
ABORTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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