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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127231111 | 12723111 | 1 | I | 20160827 | 20160908 | 20160908 | EXP | US-ZYDUS-012029 | ZYDUS PHARM | VEIZI E, TORNERO-BOLD M, HAYEK SM. RESOLUTION OF INTRATHECAL HYDROMORPHONE OR MORPHINEINDUCED PERIPHERAL EDEMA BY OPIOID ROTATION TO FENTANYL: A CASE SERIES. PAIN-PRACT 2016;16(6):E94-E98. | 67.00 | YR | E | F | Y | 0.00000 | 20160908 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127231111 | 12723111 | 1 | PS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | U | UNKNOWN | 78226 | |||||||||
| 127231111 | 12723111 | 2 | SS | TRAMADOL. | TRAMADOL | 1 | Unknown | U | UNKNOWN | 90404 | |||||||||
| 127231111 | 12723111 | 3 | SS | PREGABALIN. | PREGABALIN | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 127231111 | 12723111 | 4 | SS | HYDROMORPHONE/HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE | 1 | Intrathecal | Y | UNKNOWN | 0 | |||||||||
| 127231111 | 12723111 | 5 | SS | BUPIVACAINE. | BUPIVACAINE | 1 | Intrathecal | Y | UNKNOWN | 0 | 9.9 | MG | |||||||
| 127231111 | 12723111 | 6 | SS | HYDROMORPHONE/HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE | 1 | Intrathecal | DECREASED 32% | Y | UNKNOWN | 0 | 60 | UG | ||||||
| 127231111 | 12723111 | 7 | SS | HYDROMORPHONE/HYDROMORPHONE HYDROCHLORIDE | HYDROMORPHONE | 1 | Intrathecal | DECREASED 32% | Y | UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127231111 | 12723111 | 1 | Product used for unknown indication |
| 127231111 | 12723111 | 2 | Product used for unknown indication |
| 127231111 | 12723111 | 3 | Product used for unknown indication |
| 127231111 | 12723111 | 4 | Post laminectomy syndrome |
| 127231111 | 12723111 | 5 | Post laminectomy syndrome |
| 127231111 | 12723111 | 6 | Post laminectomy syndrome |
| 127231111 | 12723111 | 7 | Post laminectomy syndrome |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127231111 | 12723111 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127231111 | 12723111 | Device kink | |
| 127231111 | 12723111 | Oedema peripheral | |
| 127231111 | 12723111 | Pain | |
| 127231111 | 12723111 | Respiratory depression | |
| 127231111 | 12723111 | Urinary retention |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |