The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
123698892 12369889 2 F 20150114 20160712 20160516 20160714 EXP US-ALLERGAN-1656311US ALLERGAN 73.00 YR M Y 0.00000 20160714 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
123698892 12369889 1 PS COMBIGAN BRIMONIDINE TARTRATETIMOLOL MALEATE 1 Ophthalmic 2 GTT, QD Y U 21398 2 GTT EYE DROPS, SOLUTION QD
123698892 12369889 2 SS LUMIGAN BIMATOPROST 1 Ophthalmic UNK UNK, QD Y U 0 EYE DROPS, SOLUTION QD
123698892 12369889 3 C ASPIRIN. ASPIRIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123698892 12369889 1 Glaucoma
123698892 12369889 2 Glaucoma
123698892 12369889 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123698892 12369889 OT
123698892 12369889 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123698892 12369889 Dark circles under eyes
123698892 12369889 Eye irritation
123698892 12369889 Eye swelling
123698892 12369889 Hypersensitivity
123698892 12369889 Myocardial infarction
123698892 12369889 Ocular hyperaemia
123698892 12369889 Visual acuity reduced

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found