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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125824891 | 12582489 | 1 | I | 20160719 | 20160720 | 20160722 | 20160722 | EXP | BR-ROCHE-1799482 | ROCHE | 41.00 | YR | F | Y | 72.00000 | KG | 20160722 | PH | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125824891 | 12582489 | 1 | PS | MABTHERA | RITUXIMAB | 1 | Intravenous (not otherwise specified) | EVERY 15 DAYS | H0818 | 103705 | 1000 | MG | SOLUTION FOR INFUSION | ||||||
| 125824891 | 12582489 | 2 | C | DIPHENHYDRAMINE. | DIPHENHYDRAMINE | 1 | Intravenous (not otherwise specified) | 0 | 25 | MG | |||||||||
| 125824891 | 12582489 | 3 | C | DIPYRONE | DIPYRONE | 1 | Intravenous (not otherwise specified) | 0 | 1 | G | |||||||||
| 125824891 | 12582489 | 4 | C | HYDROCORTISONE. | HYDROCORTISONE | 1 | Intravenous (not otherwise specified) | 0 | 100 | MG | |||||||||
| 125824891 | 12582489 | 5 | C | CHLORPROMAZINE. | CHLORPROMAZINE | 1 | Oral | 0 | 25 | MG | TABLET | QD | |||||||
| 125824891 | 12582489 | 6 | C | CARBAMAZEPINE. | CARBAMAZEPINE | 1 | Oral | 2 TABLETS 3 TIMES A DAY | 0 | 200 | MG | TABLET | |||||||
| 125824891 | 12582489 | 7 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Oral | 0 | 20 | MG | CAPSULE | QD | |||||||
| 125824891 | 12582489 | 8 | C | AZATHIOPRINE. | AZATHIOPRINE | 1 | Oral | 0 | 50 | MG | TABLET | BID | |||||||
| 125824891 | 12582489 | 9 | C | PREDNISONE. | PREDNISONE | 1 | Oral | 0 | 20 | MG | TABLET | BID | |||||||
| 125824891 | 12582489 | 10 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | Oral | 0 | 2 | GTT | QD | ||||||||
| 125824891 | 12582489 | 11 | C | CALCIUM CARBONATE. | CALCIUM CARBONATE | 1 | Oral | 0 | 500 | MG | TABLET | QD | |||||||
| 125824891 | 12582489 | 12 | C | amitriptyline | AMITRIPTYLINE | 1 | Oral | 0 | 25 | MG | TABLET | QD | |||||||
| 125824891 | 12582489 | 13 | C | BACLOFEN. | BACLOFEN | 1 | Oral | 0 | 10 | MG | TABLET | BID | |||||||
| 125824891 | 12582489 | 14 | C | LACTULOSE. | LACTULOSE | 1 | Oral | 0 | 20 | ML | ORAL SOLUTION | BID | |||||||
| 125824891 | 12582489 | 15 | C | FLUDROCORTISONE | FLUDROCORTISONE | 1 | Oral | 0 | 50 | UG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125824891 | 12582489 | 1 | Neuromyelitis optica spectrum disorder |
| 125824891 | 12582489 | 2 | Prophylaxis |
| 125824891 | 12582489 | 3 | Prophylaxis |
| 125824891 | 12582489 | 4 | Prophylaxis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125824891 | 12582489 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125824891 | 12582489 | Laryngeal disorder | |
| 125824891 | 12582489 | Off label use | |
| 125824891 | 12582489 | Pruritus |
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 |
|---|---|---|---|---|---|---|
| 125824891 | 12582489 | 1 | 20150721 | 0 |