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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127034571 | 12703457 | 1 | I | 20160816 | 20160826 | 20160831 | 20160831 | EXP | GB-MHRA-TPP781780C2163359YC1471340227167 | GB-PFIZER INC-2016406345 | PFIZER | 32.00 | YR | M | Y | 99.00000 | KG | 20160831 | OT | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127034571 | 12703457 | 1 | PS | VARENICLINE TARTRATE | VARENICLINE TARTRATE | 1 | UNK | U | 21928 | ||||||||||
| 127034571 | 12703457 | 2 | C | NICOTINE. | NICOTINE | 1 | 1DF DAILY TO BE APPLIED | 0 | 1 | DF | QD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127034571 | 12703457 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127034571 | 12703457 | Blood pressure increased | |
| 127034571 | 12703457 | Dizziness | |
| 127034571 | 12703457 | Heart rate increased | |
| 127034571 | 12703457 | Tachycardia |
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 |
|---|---|---|---|---|---|---|
| 127034571 | 12703457 | 1 | 20160816 | 0 | ||
| 127034571 | 12703457 | 2 | 20160816 | 0 |