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

NO ADVERSE EVENT ( 36 FDA reports)
DRUG DOSE OMISSION ( 29 FDA reports)
EYE IRRITATION ( 24 FDA reports)
PRODUCT QUALITY ISSUE ( 23 FDA reports)
EYE PAIN ( 17 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 16 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 11 FDA reports)
VISION BLURRED ( 11 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 10 FDA reports)
OCULAR HYPERAEMIA ( 10 FDA reports)
EYE SWELLING ( 8 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
OFF LABEL USE ( 7 FDA reports)
PAIN ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
BURNING SENSATION ( 6 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 6 FDA reports)
BLISTER ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
INSTILLATION SITE PAIN ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
INSTILLATION SITE IRRITATION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
APPLICATION SITE PAIN ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLINDNESS TRANSIENT ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
CORNEAL EROSION ( 2 FDA reports)
ECTROPION ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EYE BURNS ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INSTILLATION SITE ERYTHEMA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PRODUCT CONTAINER ISSUE ( 2 FDA reports)
RASH ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL OPACITY ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYST ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE DERMATITIS ( 1 FDA reports)
INJECTION SITE HYPERSENSITIVITY ( 1 FDA reports)
INSTILLATION SITE ABNORMAL SENSATION ( 1 FDA reports)
INSTILLATION SITE FOREIGN BODY SENSATION ( 1 FDA reports)
INSTILLATION SITE PRURITUS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KERATORHEXIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OCULAR ROSACEA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PERIORBITAL CELLULITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRODUCT DROPPER ISSUE ( 1 FDA reports)
PRODUCT PACKAGING ISSUE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)

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