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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124693432 | 12469343 | 2 | F | 201602 | 20160815 | 20160615 | 20160831 | PER | US-TEIKOKU PHARMA USA-TPU2016-00369 | TEIKOKU | 59.45 | YR | F | Y | 88.53000 | KG | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124693432 | 12469343 | 1 | PS | LIDOCAINE PATCH | LIDOCAINE | 1 | Topical | APPLY TO LOWER BACK ONCE A DAY IN MORNING | 94118 | 20612 | QD | ||||||||
| 124693432 | 12469343 | 2 | C | TYLENOL | ACETAMINOPHEN | 1 | Oral | ONE TABLET DAILY AS NEEDED | 0 | ||||||||||
| 124693432 | 12469343 | 3 | C | MOTRIN | IBUPROFEN | 1 | Oral | ONE TABLET DAILY AS NEEDED | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124693432 | 12469343 | 1 | Back pain |
| 124693432 | 12469343 | 2 | Pain |
| 124693432 | 12469343 | 3 | Pain |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124693432 | 12469343 | Drug ineffective for unapproved indication | |
| 124693432 | 12469343 | Dysstasia | |
| 124693432 | 12469343 | Gait disturbance |
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 |
|---|---|---|---|---|---|---|
| 124693432 | 12469343 | 1 | 201411 | 0 |