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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125697101 | 12569710 | 1 | I | 20160713 | 0 | 20160718 | 20160718 | DIR | 51.00 | YR | F | N | 150.00000 | LBS | 20160716 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125697101 | 12569710 | 1 | PS | CORTISONE | CORTISONEHYDROCORTISONE | 1 | Y | D | 0 | ||||||||||
| 125697101 | 12569710 | 2 | SS | BENADRYL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | N | D | 0 |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125697101 | 12569710 | Burning sensation | |
| 125697101 | 12569710 | Erythema | |
| 125697101 | 12569710 | Fatigue | |
| 125697101 | 12569710 | Hypersensitivity | |
| 125697101 | 12569710 | Pain in extremity | |
| 125697101 | 12569710 | Pruritus | |
| 125697101 | 12569710 | Rash |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |