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
124153632 12415363 2 F 2016 20160809 20160530 20160822 PER US-PFIZER INC-2016257970 PFIZER 81.00 YR M Y 88.00000 KG 20160822 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
124153632 12415363 1 PS LATANOPROST. LATANOPROST 1 ONCE A DAY IN THE EVENING 20597 EYE DROPS, SOLUTION QD
124153632 12415363 2 SS LATANOPROST. LATANOPROST 1 Ophthalmic 1 DROP EACH EYE, NIGHTLY 20597 2 GTT EYE DROPS, SOLUTION QD
124153632 12415363 3 SS DORZOLAMIDE/TIMOLOL DORZOLAMIDETIMOLOL 1 Ophthalmic 1 DROP BOTH EYES 2X/DAY Y 0 2 GTT EYE DROPS BID
124153632 12415363 4 SS DORZOLAMIDE DORZOLAMIDE 1 UNK Y 0
124153632 12415363 5 SS TIMOLOL. TIMOLOL 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124153632 12415363 1 Glaucoma
124153632 12415363 3 Glaucoma

Outcome of event

Event ID CASEID OUTC COD
124153632 12415363 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124153632 12415363 Erythema
124153632 12415363 Eye irritation
124153632 12415363 Eye pruritus
124153632 12415363 Eye swelling
124153632 12415363 Ocular hyperaemia
124153632 12415363 Ocular hypertension
124153632 12415363 Skin irritation
124153632 12415363 Swelling face

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
124153632 12415363 1 2001 0
124153632 12415363 2 201506 20160512 0
124153632 12415363 3 20150506 20160531 0
124153632 12415363 4 20141105 20150506 0