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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127404861 | 12740486 | 1 | I | 201607 | 20160822 | 20160913 | 20160913 | PER | US-ASTRAZENECA-2016SE90566 | ASTRAZENECA | 75.00 | YR | F | Y | 68.00000 | KG | 20160914 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127404861 | 12740486 | 1 | PS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | U | U | 19810 | 25 | MG | QD | ||||||
| 127404861 | 12740486 | 2 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | Oral | OMEPRAZOLE, 25 MG ONCE A DAY | U | U | 19810 | ||||||||
| 127404861 | 12740486 | 3 | SS | CHANTIX | VARENICLINE TARTRATE | 1 | Oral | U | 00000054 | 0 | 1 | MG | TABLET | BID | |||||
| 127404861 | 12740486 | 4 | C | HIGH BLOOD PRESSURE PILL | UNSPECIFIED INGREDIENT | 1 | 0 | ||||||||||||
| 127404861 | 12740486 | 5 | C | HIGH CHOLESTEROL PILL | 2 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127404861 | 12740486 | 1 | Gastrooesophageal reflux disease |
| 127404861 | 12740486 | 2 | Gastrooesophageal reflux disease |
| 127404861 | 12740486 | 3 | Smoking cessation therapy |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127404861 | 12740486 | Drug ineffective | |
| 127404861 | 12740486 | Eructation | |
| 127404861 | 12740486 | Gastrooesophageal reflux disease | |
| 127404861 | 12740486 | Nausea |
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 |
|---|---|---|---|---|---|---|
| 127404861 | 12740486 | 3 | 201606 | 0 |