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
121310464 12131046 4 F 201602 20160614 20160301 20160705 PER US-PFIZER INC-2016111074 PFIZER 65.00 YR F Y 64.00000 KG 20160705 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
121310464 12131046 1 PS PREMPRO ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE 1 Oral 0.45-1.5 MG, 1X/DAY, IN THE EVENING L95149 20527 1 DF TABLET QD
121310464 12131046 2 SS PREMPRO ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE 1 UNK (0.45/1.5MG) M26179 20527 TABLET
121310464 12131046 3 C PROTONIX PANTOPRAZOLE SODIUM 1 40 MG, 1X/DAY, IN THE MORNING 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121310464 12131046 1 Menopausal symptoms
121310464 12131046 3 Abdominal discomfort

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121310464 12131046 Bone pain
121310464 12131046 Headache
121310464 12131046 Muscle spasms

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
121310464 12131046 2 2013 0
121310464 12131046 3 2003 0