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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126138242 | 12613824 | 2 | F | 2016 | 20160822 | 20160802 | 20160829 | EXP | US-PFIZER INC-2016336809 | PFIZER | 74.00 | YR | F | Y | 64.00000 | KG | 20160829 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126138242 | 12613824 | 1 | PS | PREMPRO | ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE | 1 | UNK(ESTROGENS CONJUGATED-0.3MG, MEDROXYPROGESTERONE ACETATE-1.5MG) | Y | M26165 | 20527 | TABLET | ||||||||
| 126138242 | 12613824 | 2 | SS | PREMPRO | ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE | 1 | UNK(ESTROGENS CONJUGATED-0.45MG, MEDROXYPROGESTERONE ACETATE-1.5MG) | Y | 20527 | TABLET | |||||||||
| 126138242 | 12613824 | 3 | SS | PREMPRO | ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE | 1 | UNK(ESTROGENS CONJUGATED-0.3MG, MEDROXYPROGESTERONE ACETATE-1.5MG) | Y | N004611051163 | 20527 | TABLET | ||||||||
| 126138242 | 12613824 | 4 | SS | PREMPHASE | ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE | 1 | UNK, 1X/DAY | Y | 20527 | TABLET | QD | ||||||||
| 126138242 | 12613824 | 5 | SS | PREMPHASE | ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE | 1 | UNK | Y | 20527 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126138242 | 12613824 | 1 | Menopausal symptoms |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126138242 | 12613824 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126138242 | 12613824 | Ageusia | |
| 126138242 | 12613824 | Alopecia | |
| 126138242 | 12613824 | Chest pain | |
| 126138242 | 12613824 | Depression | |
| 126138242 | 12613824 | Feeling abnormal | |
| 126138242 | 12613824 | Haemoptysis | |
| 126138242 | 12613824 | Headache | |
| 126138242 | 12613824 | Influenza like illness | |
| 126138242 | 12613824 | Nasopharyngitis | |
| 126138242 | 12613824 | Oropharyngeal pain | |
| 126138242 | 12613824 | Pyrexia | |
| 126138242 | 12613824 | Rhinorrhoea | |
| 126138242 | 12613824 | Sensory loss |
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 |
|---|---|---|---|---|---|---|
| 126138242 | 12613824 | 1 | 2016 | 0 | ||
| 126138242 | 12613824 | 2 | 2016 | 0 | ||
| 126138242 | 12613824 | 3 | 2016 | 0 | ||
| 126138242 | 12613824 | 4 | 2016 | 0 |