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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113196836 | 11319683 | 6 | F | 20120713 | 20160919 | 20150729 | 20160921 | PER | PHHY2014US070160 | NOVARTIS | 36.03 | YR | F | Y | 0.00000 | 20160922 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113196836 | 11319683 | 1 | PS | GILENYA | FINGOLIMOD HYDROCHLORIDE | 1 | Oral | UNK UNK, QD | 22527 | CAPSULE | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 113196836 | 11319683 | 1 | Multiple sclerosis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 113196836 | 11319683 | Abdominal pain upper | |
| 113196836 | 11319683 | Back pain | |
| 113196836 | 11319683 | Blood albumin increased | |
| 113196836 | 11319683 | Blood glucose increased | |
| 113196836 | 11319683 | Hypoaesthesia | |
| 113196836 | 11319683 | Insomnia | |
| 113196836 | 11319683 | Lymphocyte count decreased | |
| 113196836 | 11319683 | Migraine | |
| 113196836 | 11319683 | Paraesthesia | |
| 113196836 | 11319683 | Urinary tract infection | |
| 113196836 | 11319683 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |