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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125446451 | 12544645 | 1 | I | 20160706 | 20160711 | 20160711 | EXP | KP-CITRON PHARMA LLC-B16-0083-AE | CITRON | 61.00 | YR | F | Y | 0.00000 | 20160711 | MD | KP | KP |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125446451 | 12544645 | 1 | PS | FLUDROCORTISONE ACETATE. | FLUDROCORTISONE ACETATE | 1 | Unknown | 0.1 MG DAILY | U | U | 10060 | .1 | MG | TABLET | |||||
| 125446451 | 12544645 | 2 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | Unknown | 5 MG DAILY | U | U | 0 | 5 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125446451 | 12544645 | 1 | Cushing's syndrome |
| 125446451 | 12544645 | 2 | Cushing's syndrome |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125446451 | 12544645 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125446451 | 12544645 | Abdominal pain | |
| 125446451 | 12544645 | Arthralgia | |
| 125446451 | 12544645 | Arthritis infective | |
| 125446451 | 12544645 | Bronchiectasis | |
| 125446451 | 12544645 | Diarrhoea | |
| 125446451 | 12544645 | Gastroenteritis bacterial | |
| 125446451 | 12544645 | Joint swelling | |
| 125446451 | 12544645 | Pyrexia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |