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ALOPECIA ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
AGEUSIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
LIGAMENT OPERATION ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
ECZEMA WEEPING ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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