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
106925164 10692516 4 F 2014 20160822 20150106 20160829 PER US-PFIZER INC-2014363186 PFIZER 46.00 YR M Y 56.70000 KG 20160829 OT 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
106925164 10692516 1 PS LATANOPROST. LATANOPROST 1 Ophthalmic 1 DROP IN EACH EYE DAILY AT BEFORE BEDTIME Y 20597 2 GTT EYE DROPS, SOLUTION QD
106925164 10692516 2 SS LATANOPROST. LATANOPROST 1 2.5 ML, 1X/DAY (ONCE A DAY AT NIGHT BEFORE BED TIME) Y 20597 2.5 ML EYE DROPS, SOLUTION QD
106925164 10692516 3 SS LATANOPROST. LATANOPROST 1 Ophthalmic 2 GTT, 1X/DAY Y 20597 2 GTT EYE DROPS, SOLUTION QD
106925164 10692516 4 C XALATAN LATANOPROST 1 2 GTT, 1X/DAY 0 2 GTT QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106925164 10692516 1 Glaucoma
106925164 10692516 2 Optic nerve disorder

Outcome of event

Event ID CASEID OUTC COD
106925164 10692516 OT
106925164 10692516 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
106925164 10692516 Disease progression
106925164 10692516 Drug ineffective
106925164 10692516 Eye irritation
106925164 10692516 Eye pain
106925164 10692516 Glaucoma
106925164 10692516 Intraocular pressure increased

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
106925164 10692516 1 201501 0
106925164 10692516 4 20160106 0