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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105581063 | 10558106 | 3 | F | 20151020 | 20160908 | 20141031 | 20160912 | PER | US-GLAXOSMITHKLINE-US2014GSK013700 | GLAXOSMITHKLINE | 71.12 | YR | F | Y | 0.00000 | 20160912 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 105581063 | 10558106 | 1 | PS | IMITREX | SUMATRIPTAN SUCCINATE | 1 | Oral | 100 MG, PRN | U | UNKNOWN | 20132 | 100 | MG | TABLET | |||||
| 105581063 | 10558106 | 2 | SS | IMITREX | SUMATRIPTAN SUCCINATE | 1 | Nasal | UNK, U | 0 | NASAL SPRAY |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 105581063 | 10558106 | 1 | Migraine |
| 105581063 | 10558106 | 2 | Migraine |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 105581063 | 10558106 | Breast operation | |
| 105581063 | 10558106 | Drug ineffective | |
| 105581063 | 10558106 | Feeling hot | |
| 105581063 | 10558106 | Malaise | |
| 105581063 | 10558106 | Viral infection |
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 |
|---|---|---|---|---|---|---|
| 105581063 | 10558106 | 1 | 201008 | 0 | ||
| 105581063 | 10558106 | 2 | 201603 | 0 |