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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126741994 | 12674199 | 4 | F | 20160919 | 20160822 | 20160930 | PER | US-GLAXOSMITHKLINE-US2016GSK116611 | GLAXOSMITHKLINE | 0.00 | F | Y | 56.69000 | KG | 20160930 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126741994 | 12674199 | 1 | PS | IMITREX | SUMATRIPTAN SUCCINATE | 1 | U | 20080 | SOLUTION FOR INJECTION IN PRE-FILLED PEN | ||||||||||
| 126741994 | 12674199 | 2 | SS | Sumatriptan (Sumatriptan succinate) Nasal spray | SUMATRIPTAN SUCCINATE | 1 | 6 MG, UNK | Y | 0 | 6 | MG | NASAL SPRAY | |||||||
| 126741994 | 12674199 | 3 | SS | IMITREX | SUMATRIPTAN SUCCINATE | 1 | Oral | Y | 0 | TABLET | |||||||||
| 126741994 | 12674199 | 4 | C | ESTRADIOL. | ESTRADIOL | 1 | Oral | 2 MG, QD | 0 | 2 | MG | QD | |||||||
| 126741994 | 12674199 | 5 | C | PROGESTERONE. | PROGESTERONE | 1 | Oral | 200 MG, QD | 0 | 200 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126741994 | 12674199 | 1 | Migraine |
| 126741994 | 12674199 | 2 | Migraine |
| 126741994 | 12674199 | 3 | Migraine |
| 126741994 | 12674199 | 5 | Progesterone decreased |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126741994 | 12674199 | Drug dose omission | |
| 126741994 | 12674199 | Drug ineffective | |
| 126741994 | 12674199 | Drug intolerance | |
| 126741994 | 12674199 | Nausea | |
| 126741994 | 12674199 | Product quality issue | |
| 126741994 | 12674199 | Progesterone decreased | |
| 126741994 | 12674199 | Therapeutic response decreased |
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 |
|---|---|---|---|---|---|---|
| 126741994 | 12674199 | 2 | 2015 | 2015 | 0 | |
| 126741994 | 12674199 | 4 | 2010 | 0 | ||
| 126741994 | 12674199 | 5 | 2016 | 0 |