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

EYE IRRITATION ( 153 FDA reports)
DRUG INEFFECTIVE ( 83 FDA reports)
INSTILLATION SITE PAIN ( 75 FDA reports)
CONDITION AGGRAVATED ( 42 FDA reports)
OCULAR HYPERAEMIA ( 41 FDA reports)
EYE PAIN ( 37 FDA reports)
EYE PRURITUS ( 32 FDA reports)
LACRIMATION INCREASED ( 29 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 24 FDA reports)
DRUG HYPERSENSITIVITY ( 22 FDA reports)
INSTILLATION SITE IRRITATION ( 21 FDA reports)
VISION BLURRED ( 21 FDA reports)
HEADACHE ( 20 FDA reports)
DRUG EFFECT DECREASED ( 19 FDA reports)
EYELID OEDEMA ( 17 FDA reports)
DRY EYE ( 12 FDA reports)
EXPIRED DRUG ADMINISTERED ( 12 FDA reports)
MEDICATION ERROR ( 11 FDA reports)
EYE INFLAMMATION ( 10 FDA reports)
ABNORMAL SENSATION IN EYE ( 8 FDA reports)
ERYTHEMA OF EYELID ( 8 FDA reports)
EYE DISCHARGE ( 8 FDA reports)
EYE SWELLING ( 8 FDA reports)
MYDRIASIS ( 8 FDA reports)
ERYTHEMA ( 7 FDA reports)
INCORRECT DOSE ADMINISTERED ( 7 FDA reports)
OCULAR DISCOMFORT ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
EPISTAXIS ( 6 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 6 FDA reports)
PHOTOPHOBIA ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
EYELID PAIN ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
EYELID MARGIN CRUSTING ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 4 FDA reports)
RASH ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYELID DISORDER ( 3 FDA reports)
EYELID EXFOLIATION ( 3 FDA reports)
EYELID IRRITATION ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONTACT LENS INTOLERANCE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GIANT PAPILLARY CONJUNCTIVITIS ( 2 FDA reports)
HEART VALVE INCOMPETENCE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
OPHTHALMIC FLUID DRAINAGE ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN SWELLING ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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