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

MALAISE ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
COMA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
CHEST PAIN ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)

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