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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126413482 | 12641348 | 2 | F | 20160907 | 20160810 | 20160909 | PER | US-PFIZER INC-2016376149 | PFIZER | 55.00 | YR | F | Y | 72.57000 | KG | 20160909 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126413482 | 12641348 | 1 | PS | DETROL LA | TOLTERODINE TARTRATE | 1 | Oral | 4 MG, DAILY | U | C150313 | 21228 | 4 | MG | MODIFIED-RELEASE CAPSULE, SOFT | |||||
| 126413482 | 12641348 | 2 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | 40 MG, 1X/DAY | 0 | 40 | MG | QD | |||||||
| 126413482 | 12641348 | 3 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | Oral | 40 MG, 1X/DAY | 0 | 40 | MG | QD | |||||||
| 126413482 | 12641348 | 4 | C | ZOFRAN | ONDANSETRON HYDROCHLORIDE | 1 | Oral | 4 MG, 1X/DAY | 3072393 | 0 | 4 | MG | QD | ||||||
| 126413482 | 12641348 | 5 | C | ZOFRAN | ONDANSETRON HYDROCHLORIDE | 1 | 0 | ||||||||||||
| 126413482 | 12641348 | 6 | C | RANITIDINE. | RANITIDINE | 1 | Oral | 150 MG, 1X/DAY | 0 | 150 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126413482 | 12641348 | 1 | Hypertonic bladder |
| 126413482 | 12641348 | 2 | Gastrooesophageal reflux disease |
| 126413482 | 12641348 | 4 | Impaired gastric emptying |
| 126413482 | 12641348 | 5 | Gastrooesophageal reflux disease |
| 126413482 | 12641348 | 6 | Gastrooesophageal reflux disease |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126413482 | 12641348 | Drug ineffective | |
| 126413482 | 12641348 | Dry mouth | |
| 126413482 | 12641348 | Intentional product misuse | |
| 126413482 | 12641348 | Nasal dryness |
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 |
|---|---|---|---|---|---|---|
| 126413482 | 12641348 | 1 | 20160716 | 0 | ||
| 126413482 | 12641348 | 4 | 2015 | 0 | ||
| 126413482 | 12641348 | 6 | 20160531 | 0 |