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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126584882 | 12658488 | 2 | F | 20160921 | 20160817 | 20160926 | PER | PHEH2016US020613 | NOVARTIS | 0.00 | F | Y | 65.76000 | KG | 20160926 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126584882 | 12658488 | 1 | PS | ESTRADIOL. | ESTRADIOL | 1 | Transdermal | UNK, BID | 19081 | PATCH | QOW | ||||||||
| 126584882 | 12658488 | 2 | C | IMITREX | SUMATRIPTAN SUCCINATE | 1 | Unknown | UNK UNK, PRN | 0 | ||||||||||
| 126584882 | 12658488 | 3 | C | MAGNESIUM | MAGNESIUM | 1 | Unknown | UNK UNK, PRN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126584882 | 12658488 | 1 | Hysterectomy |
| 126584882 | 12658488 | 2 | Migraine |
| 126584882 | 12658488 | 3 | Migraine |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126584882 | 12658488 | Impaired healing | |
| 126584882 | 12658488 | Pruritus | |
| 126584882 | 12658488 | Skin irritation | |
| 126584882 | 12658488 | Swelling | |
| 126584882 | 12658488 | Thermal burn |
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 |
|---|---|---|---|---|---|---|
| 126584882 | 12658488 | 1 | 201602 | 0 |