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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125819771 | 12581977 | 1 | I | 20160418 | 20160722 | 20160722 | EXP | US-STRIDES ARCOLAB LIMITED-2016SP002600 | STRIDES | 0.00 | Y | 0.00000 | 20160722 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125819771 | 12581977 | 1 | PS | MYCOPHENOLATE MOFETIL. | MYCOPHENOLATE MOFETIL | 1 | Unknown | 3 G, QD | U | U | 90055 | 3 | G | ||||||
| 125819771 | 12581977 | 2 | C | PREDNISOLONE. | PREDNISOLONE | 1 | UNK | 0 | |||||||||||
| 125819771 | 12581977 | 3 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | UNK | 0 | |||||||||||
| 125819771 | 12581977 | 4 | C | COLCHICINE. | COLCHICINE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125819771 | 12581977 | 1 | Lupus nephritis |
| 125819771 | 12581977 | 2 | Product used for unknown indication |
| 125819771 | 12581977 | 3 | Basedow's disease |
| 125819771 | 12581977 | 4 | Hypersensitivity vasculitis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125819771 | 12581977 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125819771 | 12581977 | Diarrhoea | |
| 125819771 | 12581977 | Hypokalaemia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |