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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125597381 | 12559738 | 1 | I | 20160621 | 20160715 | 20160715 | PER | US-JNJFOC-20160701384 | JANSSEN | 0.00 | E | M | Y | 86.18000 | KG | 20160715 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125597381 | 12559738 | 1 | PS | TRAMADOL. | TRAMADOL | 1 | Unknown | TAKEN SIX OF THEM SINCE 18-JUN-2016 | U | 21692 | 50 | MG | UNSPECIFIED | ||||||
| 125597381 | 12559738 | 2 | SS | FAMOTIDINE. | FAMOTIDINE | 1 | Oral | U | 20325 | UNSPECIFIED | |||||||||
| 125597381 | 12559738 | 3 | SS | FAMOTIDINE. | FAMOTIDINE | 1 | Oral | U | 20325 | 20 | MG | UNSPECIFIED | BID | ||||||
| 125597381 | 12559738 | 4 | C | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Unknown | 0 | CREAM |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125597381 | 12559738 | 1 | Pain |
| 125597381 | 12559738 | 3 | Pruritus |
| 125597381 | 12559738 | 4 | Pruritus |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125597381 | 12559738 | Adverse event |
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 |
|---|---|---|---|---|---|---|
| 125597381 | 12559738 | 1 | 20160618 | 0 |