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

PYREXIA ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DEHYDRATION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
MELAENA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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