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

UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
PYREXIA ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
COUGH ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
CHILLS ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FEELING HOT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
RASH ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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