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
127420492 12742049 2 F 20160912 20160914 20160914 PER ALCN2016US006328 ALCON 0.00 M Y 104.31000 KG 20160914 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
127420492 12742049 1 PS LATANOPROST. LATANOPROST 1 Ophthalmic UNK Y U 254852F 91449
127420492 12742049 2 SS DORZOLAMIDE,TIMOLOL DORZOLAMIDETIMOLOL 1 Ophthalmic 1 GTT, BID Y U 618652 0 1 GTT EYE DROPS NOS BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127420492 12742049 1 Glaucoma
127420492 12742049 2 Glaucoma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127420492 12742049 Eye infection
127420492 12742049 Vision blurred

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127420492 12742049 1 201608 0
127420492 12742049 2 201608 0