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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127784791 | 12778479 | 1 | I | 20160321 | 20160926 | 20160926 | PER | US-PAR PHARMACEUTICAL, INC-2016SCPR015287 | PAR | 0.00 | Y | 0.00000 | 20160926 | CN | COUNTRY NOT SPECIFIED | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127784791 | 12778479 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | UNK, UNKNOWN | U | U | 70329 | ||||||||
| 127784791 | 12778479 | 2 | SS | ALEVE | NAPROXEN SODIUM | 1 | Unknown | 4-6 TABLETS, DAILY | U | U | 0 | TABLET | |||||||
| 127784791 | 12778479 | 3 | SS | IMITREX | SUMATRIPTAN SUCCINATE | 1 | Unknown | UNK, UNKNOWN | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127784791 | 12778479 | 1 | Headache |
| 127784791 | 12778479 | 2 | Headache |
| 127784791 | 12778479 | 3 | Headache |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127784791 | 12778479 | Drug administration error | |
| 127784791 | 12778479 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |