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

ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
PAIN ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
MALAISE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
INSOMNIA ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)

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