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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123766252 | 12376625 | 2 | F | 20150520 | 20150521 | 20160517 | 20160517 | PER | US-MALLINCKRODT-T201502709 | MALLINCKRODT | 58.74 | YR | F | Y | 64.00000 | KG | 20160517 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123766252 | 12376625 | 1 | PS | H.P. ACTHAR | CORTICOTROPIN | 1 | Subcutaneous | 80 UNITS, ONCE DAILY FOR 5 DAYS | 1564-69 | 8372 | INJECTION | ||||||||
| 123766252 | 12376625 | 2 | C | TOPROL XL | METOPROLOL SUCCINATE | 1 | UNK | U | 0 | ||||||||||
| 123766252 | 12376625 | 3 | C | TRIAMTERENE. | TRIAMTERENE | 1 | 37.5 MG | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123766252 | 12376625 | 1 | Multiple sclerosis relapse |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123766252 | 12376625 | Dyspnoea | |
| 123766252 | 12376625 | Hypotension | |
| 123766252 | 12376625 | Muscular weakness |
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 |
|---|---|---|---|---|---|---|
| 123766252 | 12376625 | 1 | 20150520 | 0 |