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
127361282 12736128 2 F 20160914 20160912 20160920 EXP US-PFIZER INC-2016366863 PFIZER 89.00 YR F Y 53.00000 KG 20160920 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
127361282 12736128 1 PS LATANOPROST. LATANOPROST 1 Ophthalmic 1 DROP IN EACH EYE AT BEDTIME M92831 20597 2 GTT EYE DROPS, SOLUTION
127361282 12736128 2 SS LATANOPROST. LATANOPROST 1 Ophthalmic 1 DROP IN EACH EYE AT BEDTIME M98328 20597 2 GTT EYE DROPS, SOLUTION
127361282 12736128 3 SS LATANOPROST. LATANOPROST 1 Ophthalmic 2 GTT, DAILY (1GTT OU QHS) 20597 2 GTT EYE DROPS, SOLUTION
127361282 12736128 4 C SYSTANE ULTRA POLYETHYLENE GLYCOL 400PROPYLENE GLYCOL 1 Ophthalmic ONLY DO ONE DROP IN EACH EYE A DAY 0 2 GTT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127361282 12736128 1 Intraocular pressure test abnormal
127361282 12736128 2 Glaucoma
127361282 12736128 4 Dry eye

Outcome of event

Event ID CASEID OUTC COD
127361282 12736128 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127361282 12736128 Body height decreased
127361282 12736128 Incorrect dose administered
127361282 12736128 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
127361282 12736128 2 201607 0
127361282 12736128 3 20120523 0