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
107356774 10735677 4 F 2015 20160706 20150126 20160718 EXP BR-PFIZER INC-2015021116 PFIZER 43.00 YR F Y 48.00000 KG 20160718 CN BR BR

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
107356774 10735677 1 PS XALATAN LATANOPROST 1 Ophthalmic 1 DROP IN EACH EYE EVERY DAY 3098/A089622 20597 2 GTT EYE DROPS, SOLUTION
107356774 10735677 2 SS XALATAN LATANOPROST 1 Ophthalmic 2 DROPS IN EACH EYE BEFORE SLEEPING B03098 20597 4 GTT EYE DROPS, SOLUTION QD
107356774 10735677 3 SS XALATAN LATANOPROST 1 UNK 46042 20597 EYE DROPS, SOLUTION
107356774 10735677 4 SS XALATAN LATANOPROST 1 UNK L51597 20597 EYE DROPS, SOLUTION
107356774 10735677 5 SS XALATAN LATANOPROST 1 UNK L44855 20597 EYE DROPS, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107356774 10735677 1 Glaucoma

Outcome of event

Event ID CASEID OUTC COD
107356774 10735677 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107356774 10735677 Drug ineffective
107356774 10735677 Eye discharge
107356774 10735677 Eye inflammation
107356774 10735677 Eye irritation
107356774 10735677 Intentional product use issue
107356774 10735677 Ocular hyperaemia
107356774 10735677 Product quality issue
107356774 10735677 Product use issue
107356774 10735677 Visual acuity reduced

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
107356774 10735677 1 2008 0