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

NAUSEA ( 6 FDA reports)
RENAL FAILURE ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
DISORIENTATION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
INJURY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
URTICARIA PIGMENTOSA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
DEATH ( 1 FDA reports)

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