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

TACHYCARDIA ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
ARTHRALGIA ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
SYNCOPE ( 2 FDA reports)
SOPOR ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
RASH ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
MINERAL SUPPLEMENTATION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERONEGATIVE ARTHRITIS ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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