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
125746672 12574667 2 F 20160604 20160802 20160720 20160804 EXP NL-LRB-222385 NL-PFIZER INC-2016351203 PFIZER 35.00 YR F Y 71.00000 KG 20160804 CN NL NL

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
125746672 12574667 1 PS PROVERA MEDROXYPROGESTERONE ACETATE 1 Oral 10 MG, 2X/DAY Y 11839 10 MG TABLET BID
125746672 12574667 2 SS PROVERA MEDROXYPROGESTERONE ACETATE 1 20 MG, 2X/DAY Y 11839 20 MG TABLET BID
125746672 12574667 3 C SOTALOL. SOTALOL 1 Oral 80 MG, 2X/DAY 0 80 MG BID
125746672 12574667 4 C SOTALOL. SOTALOL 1 Oral 80 MG, 3X/DAY 0 80 MG TID
125746672 12574667 5 C EUTHYROX LEVOTHYROXINE SODIUM 1 Oral 112 UG, 1X/DAY 0 112 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125746672 12574667 1 Contraception

Outcome of event

Event ID CASEID OUTC COD
125746672 12574667 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125746672 12574667 Arrhythmia
125746672 12574667 Product use 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
125746672 12574667 1 20160604 0
125746672 12574667 2 20160713 0
125746672 12574667 3 2013 201603 0
125746672 12574667 4 201604 0
125746672 12574667 5 2014 0