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
126257371 12625737 1 I 2009 20160525 20160805 20160805 EXP US-PFIZER INC-2016276591 PFIZER 0.00 F Y 0.00000 20160805 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
126257371 12625737 1 PS PREMARIN ESTROGENS, CONJUGATED 1 UNK UNK, DAILY Y 4782 TABLET
126257371 12625737 2 SS PREMARIN ESTROGENS, CONJUGATED 1 Vaginal 0.625 MG, 2X/WEEK Y 20216 .625 MG VAGINAL CREAM BIW
126257371 12625737 3 C LYRICA PREGABALIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126257371 12625737 1 Hormone replacement therapy
126257371 12625737 2 Atrophic vulvovaginitis

Outcome of event

Event ID CASEID OUTC COD
126257371 12625737 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126257371 12625737 Drug dispensing error
126257371 12625737 Headache
126257371 12625737 Intentional product misuse
126257371 12625737 Intervertebral disc degeneration
126257371 12625737 Nausea
126257371 12625737 Peripheral swelling
126257371 12625737 Swelling face
126257371 12625737 Vaginal haemorrhage
126257371 12625737 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
126257371 12625737 1 1995 0