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

HYPOGLYCAEMIA ( 15 FDA reports)
DRUG INTERACTION ( 12 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEADACHE ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
URTICARIA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
ACANTHOSIS NIGRICANS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
CUTANEOUS AMYLOIDOSIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY ( 1 FDA reports)
COUGH ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use