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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121267883 | 12126788 | 3 | F | 20150901 | 20160628 | 20160229 | 20160705 | EXP | US-BIOGEN-2015BI112131 | BIOGEN | 39.88 | YR | F | Y | 0.00000 | 20160705 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121267883 | 12126788 | 1 | PS | TYSABRI | NATALIZUMAB | 1 | Intravenous (not otherwise specified) | 125104 | 300 | MG | CONCENTRATE FOR SOLUTION FOR INFUSION | /month | |||||||
| 121267883 | 12126788 | 2 | C | NEURONTIN | GABAPENTIN | 1 | Unknown | 0 | 300 | MG | UNKNOWN | QD | |||||||
| 121267883 | 12126788 | 3 | C | TIZANIDINE. | TIZANIDINE | 1 | Unknown | 0 | 4 | MG | UNKNOWN | Q8H | |||||||
| 121267883 | 12126788 | 4 | C | ALPRAZOLAM. | ALPRAZOLAM | 1 | Unknown | 0 | .25 | MG | UNKNOWN | TID | |||||||
| 121267883 | 12126788 | 5 | C | VICODIN | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | Unknown | 0 | UNKNOWN | ||||||||||
| 121267883 | 12126788 | 6 | C | Morphine | MORPHINE | 1 | Unknown | 0 | UNKNOWN |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121267883 | 12126788 | 1 | Multiple sclerosis |
| 121267883 | 12126788 | 2 | Product used for unknown indication |
| 121267883 | 12126788 | 3 | Product used for unknown indication |
| 121267883 | 12126788 | 4 | Product used for unknown indication |
| 121267883 | 12126788 | 5 | Product used for unknown indication |
| 121267883 | 12126788 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 121267883 | 12126788 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121267883 | 12126788 | Abortion spontaneous | |
| 121267883 | 12126788 | Maternal 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 |
|---|---|---|---|---|---|---|
| 121267883 | 12126788 | 1 | 20150727 | 20150727 | 0 |