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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125695941 | 12569594 | 1 | I | 20160708 | 20160719 | 20160719 | EXP | CA-PURDUE-CAN-2016-0006872 | PURDUE | 36.00 | YR | F | Y | 75.00000 | KG | 20160713 | CN | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125695941 | 12569594 | 1 | PS | HYDROMORPHONE HCL | HYDROMORPHONE HYDROCHLORIDE | 1 | Oral | 2 MG, DAILY | U | U | 19892 | 2 | MG | ||||||
| 125695941 | 12569594 | 2 | SS | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Oral | 30 MG, DAILY | U | U | 0 | 30 | MG | CAPSULE | |||||
| 125695941 | 12569594 | 3 | SS | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Oral | 40 MG, DAILY | U | U | 0 | 40 | MG | ||||||
| 125695941 | 12569594 | 4 | C | SENOKOT | SENNOSIDES | 1 | Unknown | UNK | U | U | 0 | TABLET | |||||||
| 125695941 | 12569594 | 5 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 125695941 | 12569594 | 6 | C | NAPROXEN. | NAPROXEN | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125695941 | 12569594 | 1 | Pain |
| 125695941 | 12569594 | 2 | Pain |
| 125695941 | 12569594 | 3 | Prophylaxis against gastrointestinal ulcer |
| 125695941 | 12569594 | 4 | Product used for unknown indication |
| 125695941 | 12569594 | 5 | Product used for unknown indication |
| 125695941 | 12569594 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125695941 | 12569594 | HO |
| 125695941 | 12569594 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125695941 | 12569594 | Anaphylactic shock | |
| 125695941 | 12569594 | Dysphagia | |
| 125695941 | 12569594 | Dyspnoea | |
| 125695941 | 12569594 | Pharyngeal oedema | |
| 125695941 | 12569594 | Pruritus | |
| 125695941 | 12569594 | Rash erythematous | |
| 125695941 | 12569594 | Rash generalised | |
| 125695941 | 12569594 | Rash papular | |
| 125695941 | 12569594 | Skin burning sensation | |
| 125695941 | 12569594 | Skin reaction | |
| 125695941 | 12569594 | Swelling face |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |