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

OCULAR HYPERAEMIA ( 13 FDA reports)
EYE IRRITATION ( 11 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
FALL ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
MARROW HYPERPLASIA ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
DIZZINESS ( 3 FDA reports)
EPISCLERITIS ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
RASH ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BACTERIAL DISEASE CARRIER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATARACT OPERATION COMPLICATION ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CORNEAL SCAR ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG THERAPY CHANGED ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ENTEROCOLITIS VIRAL ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYELID BLEEDING ( 2 FDA reports)
FELTY'S SYNDROME ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HYPERPARATHYROIDISM TERTIARY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
LABILE HYPERTENSION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MADAROSIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PITYRIASIS RUBRA PILARIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RADICULITIS ( 2 FDA reports)
REHABILITATION THERAPY ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SCLERAL HYPERAEMIA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPINAL LIGAMENT OSSIFICATION ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
UVEITIS ( 1 FDA reports)

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