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
126508501 12650850 1 I 20160601 0 20160812 20160812 DIR 69.00 YR F N 130.00000 LBS 20160811 Y 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
126508501 12650850 1 PS LATANOPROST. LATANOPROST 1 Ophthalmic INOT THE EYE Y Y M46113,M46375 20180501 0 1 GTT HS
126508501 12650850 3 C CALCIUM CALCIUM 1 0
126508501 12650850 5 C PROBIOTICS PROBIOTICS NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126508501 12650850 1 Intraocular pressure test abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126508501 12650850 Accidental exposure to product
126508501 12650850 Accidental overdose
126508501 12650850 Device issue
126508501 12650850 Eye pain
126508501 12650850 Eyelid margin crusting
126508501 12650850 Overdose
126508501 12650850 Product substitution issue

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
126508501 12650850 1 20160201 20160801 0