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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126996822 | 12699682 | 2 | F | 2016 | 20160923 | 20160830 | 20160926 | EXP | US-JNJFOC-20160825240 | JANSSEN | 0.00 | A | F | Y | 117.94000 | KG | 20160926 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126996822 | 12699682 | 1 | PS | FENTANYL. | FENTANYL | 1 | Transdermal | Y | N | UNKNOWN | 19813 | UNSPECIFIED | |||||||
| 126996822 | 12699682 | 2 | C | CYCLOBENZAPRINE | CYCLOBENZAPRINE | 1 | Oral | D | 0 | 5 | MG | UNSPECIFIED | Q8H | ||||||
| 126996822 | 12699682 | 3 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Oral | 100,000 | D | 0 | UNSPECIFIED | ||||||||
| 126996822 | 12699682 | 4 | C | GABAPENTIN. | GABAPENTIN | 1 | Oral | D | 0 | 300 | MG | UNSPECIFIED | TID | ||||||
| 126996822 | 12699682 | 5 | C | MORPHINE | MORPHINE | 1 | Oral | ^UP 10 A DAY^ | D | 0 | 30 | MG | TABLETS | ||||||
| 126996822 | 12699682 | 6 | C | BUSPIRONE | BUSPIRONE HYDROCHLORIDE | 1 | Oral | 1/2 TABLET | D | 0 | 7.5 | MG | TABLET | BID | |||||
| 126996822 | 12699682 | 7 | C | OXYCODONE | OXYCODONE | 1 | Oral | D | 0 | 10 | MG | UNSPECIFIED | Q6H | ||||||
| 126996822 | 12699682 | 8 | C | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Oral | D | 0 | 200 | MG | UNSPECIFIED | |||||||
| 126996822 | 12699682 | 9 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Oral | D | 0 | 500 | MG | UNSPECIFIED | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126996822 | 12699682 | 1 | Product used for unknown indication |
| 126996822 | 12699682 | 2 | Muscle relaxant therapy |
| 126996822 | 12699682 | 5 | Pain |
| 126996822 | 12699682 | 8 | Depression |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126996822 | 12699682 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126996822 | 12699682 | Drug dose omission | |
| 126996822 | 12699682 | Drug ineffective | |
| 126996822 | 12699682 | Knee arthroplasty | |
| 126996822 | 12699682 | Product quality issue | |
| 126996822 | 12699682 | Sleep apnoea syndrome |
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 |
|---|---|---|---|---|---|---|
| 126996822 | 12699682 | 1 | 2016 | 2016 | 0 |