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
125651763 12565176 3 F 20160413 20160822 20160718 20160825 EXP US-PFIZER INC-2016338605 PFIZER 75.00 YR F Y 58.00000 KG 20160825 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
125651763 12565176 1 PS PREMARIN ESTROGENS, CONJUGATED 1 1.06 OUNCES, SHE SUPPOSED TO USE IN EVERY NIGHT FOR TWO WEEKS Y M48229 20216 VAGINAL CREAM
125651763 12565176 2 SS PREMARIN ESTROGENS, CONJUGATED 1 (0.625) Y M48229 20216 VAGINAL CREAM
125651763 12565176 3 C ATORVASTATIN ATORVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125651763 12565176 1 Vaginal infection
125651763 12565176 2 Vulvovaginal discomfort

Outcome of event

Event ID CASEID OUTC COD
125651763 12565176 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125651763 12565176 Drug ineffective for unapproved indication
125651763 12565176 Vulvovaginal burning sensation
125651763 12565176 Vulvovaginal pain

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
125651763 12565176 1 20160413 0
125651763 12565176 2 20160413 201604 0