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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127685421 | 12768542 | 1 | I | 201609 | 20160914 | 20160921 | 20160921 | PER | US-TEIKOKU PHARMA USA-TPU2016-00611 | TEIKOKU | 64.34 | YR | F | Y | 59.02000 | KG | 20160921 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127685421 | 12768542 | 1 | PS | LIDODERM | LIDOCAINE | 1 | Topical | 45038 | 20612 | Q12H |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127685421 | 12768542 | 1 | Injury |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127685421 | 12768542 | Dizziness | |
| 127685421 | 12768542 | Feeling abnormal | |
| 127685421 | 12768542 | Inappropriate schedule of drug administration | |
| 127685421 | 12768542 | Incorrect drug administration duration | |
| 127685421 | 12768542 | Malaise | |
| 127685421 | 12768542 | Nausea | |
| 127685421 | 12768542 | Palpitations |
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 |
|---|---|---|---|---|---|---|
| 127685421 | 12768542 | 1 | 2015 | 0 |