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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126065671 | 12606567 | 1 | I | 20160718 | 20160729 | 20160729 | EXP | NL-TEVA-679182ISR | TEVA | LAREB. TOPICAL CORTICOSTEROIDS AND STEROID WITHDRAWAL SYNDROME IN ATOPIC ECZEMA LAREB-QUART-REP 2016;:. | 4.00 | DEC | F | Y | 0.00000 | 20160729 | OT | NL | NL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126065671 | 12606567 | 1 | PS | HYDROCORTISONE. | HYDROCORTISONE | 1 | Topical | 80400 | |||||||||||
| 126065671 | 12606567 | 2 | SS | mometasone | MOMETASONE | 1 | Topical | 1 MG/G | 0 | ||||||||||
| 126065671 | 12606567 | 3 | C | TACROLIMUS. | TACROLIMUS | 1 | Unknown | 0.3 MG/G | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126065671 | 12606567 | 1 | Eczema |
| 126065671 | 12606567 | 2 | Eczema |
| 126065671 | 12606567 | 3 | Eczema |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126065671 | 12606567 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126065671 | 12606567 | Steroid withdrawal syndrome |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |