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

PNEUMONIA ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
ACUTE TONSILLITIS ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
RHINITIS ( 6 FDA reports)
REFLUX OESOPHAGITIS ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
CONJUNCTIVITIS ( 6 FDA reports)
CROUP INFECTIOUS ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
RASH ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
FEBRILE CONVULSION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
URTICARIA GENERALISED ( 2 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)

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