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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127745301 | 12774530 | 1 | I | 20120123 | 20120503 | 20160923 | 20160923 | EXP | BR-EMD SERONO-7130524 | EMD SERONO INC | 43.24 | YR | M | Y | 0.00000 | 20160923 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127745301 | 12774530 | 1 | PS | REBIF | INTERFERON BETA-1A | 1 | Subcutaneous | 103780 | 44 | UG | INJECTION | TIW | |||||||
| 127745301 | 12774530 | 2 | SS | REBIF | INTERFERON BETA-1A | 1 | Subcutaneous | RESUMED | 103780 | 44 | UG | INJECTION | TIW | ||||||
| 127745301 | 12774530 | 3 | C | PARACETAMOL | ACETAMINOPHEN | 1 | 0 | ||||||||||||
| 127745301 | 12774530 | 4 | C | ATENOLOL. | ATENOLOL | 1 | 0 | ||||||||||||
| 127745301 | 12774530 | 5 | C | SIMVASTATIN. | SIMVASTATIN | 1 | 0 | ||||||||||||
| 127745301 | 12774530 | 6 | C | AMIODARONE | AMIODARONE | 1 | 0 | ||||||||||||
| 127745301 | 12774530 | 7 | C | AAS | ASPIRIN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127745301 | 12774530 | 1 | Relapsing-remitting multiple sclerosis |
| 127745301 | 12774530 | 3 | Product used for unknown indication |
| 127745301 | 12774530 | 4 | Product used for unknown indication |
| 127745301 | 12774530 | 5 | Product used for unknown indication |
| 127745301 | 12774530 | 6 | Product used for unknown indication |
| 127745301 | 12774530 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127745301 | 12774530 | HO |
| 127745301 | 12774530 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127745301 | 12774530 | Breast pain | |
| 127745301 | 12774530 | Cardiac arrest | |
| 127745301 | 12774530 | Myalgia | |
| 127745301 | 12774530 | Myocardial infarction | |
| 127745301 | 12774530 | Tooth disorder |
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 |
|---|---|---|---|---|---|---|
| 127745301 | 12774530 | 1 | 20080801 | 20120103 | 0 | |
| 127745301 | 12774530 | 2 | 20120419 | 0 |