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

INFUSION RELATED REACTION ( 15 FDA reports)
MEDICATION ERROR ( 14 FDA reports)
DYSPNOEA ( 9 FDA reports)
HYPOTENSION ( 9 FDA reports)
ANAPHYLACTOID REACTION ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
PRURITUS ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
RASH ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE IRRITATION ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CLEFT LIP ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INAPPROPRIATE DEVICE PROGRAMMING ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFUSION SITE EXFOLIATION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)

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