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

SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
ILEUS ( 3 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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