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

NAUSEA ( 5 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
STRESS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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