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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125670191 | 12567019 | 1 | I | 20160629 | 20160713 | 20160718 | 20160718 | EXP | PHEH2016US017606 | NOVARTIS | 69.89 | YR | F | Y | 65.77000 | KG | 20160718 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125670191 | 12567019 | 1 | PS | ESTRADIOL. | ESTRADIOL | 1 | Transdermal | 0.1 MG, Q72H | Y | U | 77508 | 19081 | .1 | MG | PATCH |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125670191 | 12567019 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125670191 | 12567019 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125670191 | 12567019 | Anger | |
| 125670191 | 12567019 | Disorientation | |
| 125670191 | 12567019 | Headache | |
| 125670191 | 12567019 | Hot flush | |
| 125670191 | 12567019 | Mood swings | |
| 125670191 | 12567019 | Night sweats |
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 |
|---|---|---|---|---|---|---|
| 125670191 | 12567019 | 1 | 20160629 | 0 |