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
125424053 12542405 3 F 20160523 20160824 20160708 20160826 EXP ALCN2016US004562 ALCON 89.00 YR M Y 111.11000 KG 20160826 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
125424053 12542405 1 PS LATANOPROST. LATANOPROST 1 Ophthalmic UNK GTT, QHS Y N 261101F 91449
125424053 12542405 2 C ADVIL IBUPROFEN 1 Unknown U 0
125424053 12542405 3 C CLARITIN-D 12 HOUR LORATADINEPSEUDOEPHEDRINE SULFATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125424053 12542405 1 Intraocular pressure increased
125424053 12542405 2 Product used for unknown indication
125424053 12542405 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125424053 12542405 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125424053 12542405 Blindness transient
125424053 12542405 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
125424053 12542405 1 20160523 20160624 0