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VASCULITIS ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)

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