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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127416171 | 12741617 | 1 | I | 20160824 | 20160831 | 20160914 | 20160914 | EXP | US-ACORDA-ACO_127948_2016 | ACORDA | 56.00 | YR | F | Y | 0.00000 | 20160914 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127416171 | 12741617 | 1 | PS | AMPYRA | DALFAMPRIDINE | 1 | Oral | 10 MG, Q 12 HRS | VBZS | 22250 | 10 | MG | TABLET | Q12H | |||||
127416171 | 12741617 | 2 | C | GLATOPA | GLATIRAMER ACETATE | 1 | Unknown | UNK | U | 0 | |||||||||
127416171 | 12741617 | 3 | C | BACLOFEN. | BACLOFEN | 1 | Unknown | UNK | U | 0 | |||||||||
127416171 | 12741617 | 4 | C | SINEMET CR | CARBIDOPALEVODOPA | 1 | Unknown | UNK | U | 0 | |||||||||
127416171 | 12741617 | 5 | C | LISINOPRIL. | LISINOPRIL | 1 | Unknown | UNK | U | 0 | |||||||||
127416171 | 12741617 | 6 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127416171 | 12741617 | 1 | Multiple sclerosis |
127416171 | 12741617 | 2 | Product used for unknown indication |
127416171 | 12741617 | 3 | Product used for unknown indication |
127416171 | 12741617 | 4 | Product used for unknown indication |
127416171 | 12741617 | 5 | Product used for unknown indication |
127416171 | 12741617 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127416171 | 12741617 | HO |
127416171 | 12741617 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127416171 | 12741617 | Escherichia test positive | |
127416171 | 12741617 | Laboratory test abnormal | |
127416171 | 12741617 | Postictal paralysis | |
127416171 | 12741617 | Seizure |
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 |
---|---|---|---|---|---|---|
127416171 | 12741617 | 1 | 201011 | 201608 | 0 |