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

COUGH ( 5 FDA reports)
TONSILLAR ULCER ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
TONSILLAR HYPERTROPHY ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
PHARYNGEAL ERYTHEMA ( 4 FDA reports)
PALLOR ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTRAOCULAR LENS IMPLANT ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MASS ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NODULE ( 2 FDA reports)
EYE OPERATION ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
CYSTOCELE ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RECTOCELE ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
MALAISE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)

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