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

PRESCRIBED OVERDOSE ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
LACERATION ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GLOBULIN URINE PRESENT ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)

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