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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127317011 | 12731701 | 1 | I | 20160902 | 20160912 | 20160912 | PER | US-PFIZER INC-2016417235 | PFIZER | 0.00 | M | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127317011 | 12731701 | 1 | PS | TIKOSYN | DOFETILIDE | 1 | U | 20931 | CAPSULE, HARD | ||||||||||
| 127317011 | 12731701 | 2 | C | TYLENOL PM | ACETAMINOPHENDIPHENHYDRAMINE | 1 | UNK | 0 | |||||||||||
| 127317011 | 12731701 | 3 | C | ADVIL PM | DIPHENHYDRAMINE CITRATEIBUPROFEN | 1 | UNK | 0 | |||||||||||
| 127317011 | 12731701 | 4 | C | ZOLPIDEM | ZOLPIDEMOLPIDEM TARTRATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127317011 | 12731701 | 2 | Sleep disorder |
| 127317011 | 12731701 | 3 | Sleep disorder |
| 127317011 | 12731701 | 4 | Sleep disorder |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127317011 | 12731701 | Cough | |
| 127317011 | 12731701 | Head discomfort | |
| 127317011 | 12731701 | Headache |
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 |
|---|---|---|---|---|---|---|
| 127317011 | 12731701 | 1 | 201503 | 0 |