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
125524771 12552477 1 I 201601 20160711 20160713 20160713 PER US-PFIZER INC-2016341459 PFIZER 64.00 YR F Y 59.00000 KG 20160713 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
125524771 12552477 1 PS PREMARIN ESTROGENS, CONJUGATED 1 Vaginal 1 G, 1X/DAY FOR 7 DAYS 20216 1 G VAGINAL CREAM QD
125524771 12552477 2 SS PREMARIN ESTROGENS, CONJUGATED 1 Vaginal 1 G, 2X/WEEK 20216 1 G VAGINAL CREAM BIW
125524771 12552477 3 SS PREMARIN ESTROGENS, CONJUGATED 1 20216 VAGINAL CREAM
125524771 12552477 4 SS PREMARIN ESTROGENS, CONJUGATED 1 20216 VAGINAL CREAM
125524771 12552477 5 SS PREMARIN ESTROGENS, CONJUGATED 1 20216 VAGINAL CREAM
125524771 12552477 6 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125524771 12552477 1 Hormone therapy
125524771 12552477 2 Atrophic vulvovaginitis
125524771 12552477 3 Pain
125524771 12552477 4 Burning sensation
125524771 12552477 5 Pruritus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125524771 12552477 Activities of daily living impaired
125524771 12552477 Drug effect incomplete
125524771 12552477 Drug ineffective
125524771 12552477 Malaise

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
125524771 12552477 1 20160113 0