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
125199944 12519994 4 F 201601 20160919 20160630 20160923 EXP US-PFIZER INC-2016288273 PFIZER 65.00 YR F Y 80.00000 KG 20160923 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
125199944 12519994 1 PS ARTHROTEC DICLOFENAC SODIUMMISOPROSTOL 1 Oral 200 UG/75 MG, 2X/DAY 306969 20607 TABLET BID
125199944 12519994 2 SS ARTHROTEC DICLOFENAC SODIUMMISOPROSTOL 1 200 UG/50 MG 20607 TABLET
125199944 12519994 3 SS ARTHROTEC DICLOFENAC SODIUMMISOPROSTOL 1 50 MG, UNK 20607 50 MG TABLET
125199944 12519994 4 SS ARTHROTEC DICLOFENAC SODIUMMISOPROSTOL 1 75 MG, UNK 20607 75 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125199944 12519994 1 Inflammatory pain

Outcome of event

Event ID CASEID OUTC COD
125199944 12519994 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125199944 12519994 Intentional underdose
125199944 12519994 Meniscus injury

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
125199944 12519994 4 20160907 0