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
121965623 12196562 3 F 20160316 20160712 20160321 20160719 EXP US-PFIZER INC-2016166154 PFIZER 60.00 YR F Y 113.00000 KG 20160719 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
121965623 12196562 1 PS PREMARIN ESTROGENS, CONJUGATED 1 0.625MG, SINGLE DOSE, SUPPOSED 0.625MG 2X/WEEK Y M14153 20216 .625 MG VAGINAL CREAM
121965623 12196562 2 SS PREMARIN ESTROGENS, CONJUGATED 1 0.625MG, SINGLE DOSE, SUPPOSED 0.625MG 2X/WEEK Y RX487-487 20216 .625 MG VAGINAL CREAM
121965623 12196562 3 SS PREMARIN ESTROGENS, CONJUGATED 1 Y 20216 VAGINAL CREAM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121965623 12196562 1 Vulvovaginal dryness
121965623 12196562 2 Oestrogen deficiency
121965623 12196562 3 Pruritus

Outcome of event

Event ID CASEID OUTC COD
121965623 12196562 OT
121965623 12196562 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121965623 12196562 Blood pressure increased
121965623 12196562 Discomfort
121965623 12196562 Kidney infection
121965623 12196562 Pain
121965623 12196562 Pruritus generalised
121965623 12196562 Urticaria

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
121965623 12196562 1 20160316 0