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

PYREXIA ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
VOMITING ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
COMA ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SWELLING ( 1 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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