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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126995163 | 12699516 | 3 | F | 20160723 | 20160830 | 20160830 | 20160912 | EXP | US-JUBILANT CADISTA PHARMACEUTICALS-2016JUB00312 | JUBILANT | 22.26 | YR | F | Y | 86.00000 | KG | 20160912 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126995163 | 12699516 | 1 | PS | MYCOPHENOLATE MOFETIL. | MYCOPHENOLATE MOFETIL | 1 | Oral | 1500 MG, 1X/DAY | 90661 | 1500 | MG | QD | |||||||
| 126995163 | 12699516 | 2 | SS | MYCOPHENOLATE MOFETIL. | MYCOPHENOLATE MOFETIL | 1 | Oral | 1000 MG, 1X/DAY | 90661 | 1000 | MG | QD | |||||||
| 126995163 | 12699516 | 3 | C | HYDROXYCHLOROQUINE SULFATE. | HYDROXYCHLOROQUINE SULFATE | 1 | 200 MG, 2X/DAY | 0 | 200 | MG | BID | ||||||||
| 126995163 | 12699516 | 4 | C | CALCIUM WITH VITAMIN D | CALCIUMVITAMIN D | 1 | 1 TABLETS, 2X/DAY | 0 | 1 | DF | BID | ||||||||
| 126995163 | 12699516 | 5 | C | FERROUS SULFATE. | FERROUS SULFATE | 1 | 325 MG, 1X/DAY | 0 | 325 | MG | QD | ||||||||
| 126995163 | 12699516 | 6 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 20 MG, 1X/DAY | 0 | 20 | MG | QD | ||||||||
| 126995163 | 12699516 | 7 | C | LOSARTAN POTASSIUM. | LOSARTAN POTASSIUM | 1 | 100 MG, 1X/DAY | 0 | 100 | MG | QD | ||||||||
| 126995163 | 12699516 | 8 | C | MICRONOR | NORETHINDRONE | 1 | 0.35 MG, 1X/DAY | 0 | .35 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126995163 | 12699516 | 1 | Lupus nephritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126995163 | 12699516 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126995163 | 12699516 | Exposure during pregnancy |
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 |
|---|---|---|---|---|---|---|
| 126995163 | 12699516 | 1 | 2014 | 20160725 | 0 | |
| 126995163 | 12699516 | 2 | 2014 | 20160725 | 0 | |
| 126995163 | 12699516 | 3 | 2012 | 0 | ||
| 126995163 | 12699516 | 4 | 2012 | 0 | ||
| 126995163 | 12699516 | 6 | 2012 | 0 | ||
| 126995163 | 12699516 | 7 | 2012 | 20160725 | 0 | |
| 126995163 | 12699516 | 8 | 2012 | 0 |