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

MASS ( 6 FDA reports)
VITREOUS HAEMORRHAGE ( 6 FDA reports)
CYTOLYTIC HEPATITIS ( 6 FDA reports)
BLINDNESS UNILATERAL ( 6 FDA reports)
UNDERDOSE ( 6 FDA reports)
NAUSEA ( 5 FDA reports)
HEADACHE ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
ASCITES ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FACE OEDEMA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)

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