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

ABNORMAL BEHAVIOUR ( 12 FDA reports)
DELIRIUM ( 12 FDA reports)
AGITATION ( 6 FDA reports)
RASH ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
URTICARIA ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
RASH GENERALISED ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
FALL ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
POSTICTAL PARALYSIS ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEHYDRATION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
FEAR ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use