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

FATIGUE ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DIPLOPIA ( 3 FDA reports)
HAEMATOMA ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)

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