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
126177541 12617754 1 I 20160801 20160803 20160803 PER US-PFIZER INC-2016371726 PFIZER 58.00 YR F Y 0.00000 20160803 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
126177541 12617754 1 PS PREMPRO ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE 1 Oral 0.03 MG AND 1.5, 1X/DAY EVERY MORNING U 20527 TABLET QD
126177541 12617754 2 SS PREMPRO ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE 1 U 20527 TABLET
126177541 12617754 3 SS PREMPRO ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE 1 U 20527 TABLET
126177541 12617754 4 C METOPROLOL. METOPROLOL 1 25 MG, 2X/DAY 0 25 MG BID
126177541 12617754 5 C AMLODIPINE AMLODIPINE BESYLATE 1 10 MG, 1X/DAY 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126177541 12617754 1 Vulvovaginal dryness
126177541 12617754 2 Oestrogen therapy
126177541 12617754 3 Postmenopause
126177541 12617754 4 Hypertension
126177541 12617754 5 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126177541 12617754 Weight increased

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
126177541 12617754 1 20160628 0