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
124970443 12497044 3 F 201606 20160810 20160624 20160818 PER ALCN2016US004420 ALCON 81.46 YR F Y 0.00000 20160818 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
124970443 12497044 1 PS TIMOLOL. TIMOLOL 1 Ophthalmic 1 GTT, BID U 263392F 74262 1 GTT BID
124970443 12497044 2 SS LATANOPROST. LATANOPROST 1 Ophthalmic 1 GTT, UNK 254857F 0 1 GTT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124970443 12497044 1 Glaucoma
124970443 12497044 2 Glaucoma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124970443 12497044 Eye irritation
124970443 12497044 Foreign body sensation in eyes
124970443 12497044 Wrong patient received medication

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
124970443 12497044 1 201606 20160623 0