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
127088332 12708833 2 F 20160831 20160901 20160907 PER US-PFIZER INC-2016349897 PFIZER 68.00 YR F Y 0.00000 20160907 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
127088332 12708833 1 PS LATANOPROST. LATANOPROST 1 Ophthalmic 1 DROP IN EACH EYE, 1X/DAY AT BEDTIME M46113 20597 2 GTT EYE DROPS, SOLUTION QD
127088332 12708833 2 SS LATANOPROST. LATANOPROST 1 UNK M46374 20597 EYE DROPS, SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127088332 12708833 1 Intraocular pressure test abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127088332 12708833 Eye pain
127088332 12708833 Incorrect dose administered
127088332 12708833 Medication residue present
127088332 12708833 Poor quality drug administered
127088332 12708833 Product quality issue

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
127088332 12708833 1 20160701 0