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

WEIGHT INCREASED ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
PUPILLARY DISORDER ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DERMOID CYST ( 2 FDA reports)
CYST RUPTURE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHILLS ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
COUGH ( 1 FDA reports)
CATARACT ( 1 FDA reports)
DEATH ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)

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