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

ASTHENIA ( 3 FDA reports)
PAIN ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
TREMOR ( 2 FDA reports)
STRESS ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
MALAISE ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
FALL ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DERMAL SINUS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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