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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
106851245 | 10685124 | 5 | F | 20160303 | 20141231 | 20160331 | PER | US-PFIZER INC-2014352618 | PFIZER | 62.00 | YR | F | Y | 59.00000 | KG | 20160331 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
106851245 | 10685124 | 1 | PS | PREMARIN | ESTROGENS, CONJUGATED | 1 | 1GR FOR 2WKS | 20216 | 1 | G | VAGINAL CREAM | ||||||||
106851245 | 10685124 | 2 | SS | PREMARIN | ESTROGENS, CONJUGATED | 1 | 1 G, 2X/WEEK (1GM TWICE A WEEK) | L94897 | 20216 | 1 | G | VAGINAL CREAM | BIW |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
106851245 | 10685124 | 1 | Oestrogen therapy |
106851245 | 10685124 | 2 | Menopause |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
106851245 | 10685124 | Drug effect decreased | |
106851245 | 10685124 | Incorrect dose administered | |
106851245 | 10685124 | Product quality issue |
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 |
---|---|---|---|---|---|---|
106851245 | 10685124 | 1 | 2011 | 0 |