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

AMNESIA ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
FALL ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
CHEST PAIN ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
ANXIETY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
FEAR OF FALLING ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION SITE BRUISING ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOCAL REACTION ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COMA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FEAR ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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