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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
93423104 | 9342310 | 4 | F | 20130530 | 20160719 | 20130611 | 20160722 | EXP | PHHY2013CA056631 | NOVARTIS | 37.64 | YR | F | Y | 0.00000 | 20160722 | CN | CA | CA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
93423104 | 9342310 | 1 | PS | GILENYA | FINGOLIMOD HYDROCHLORIDE | 1 | Oral | 0.5 MG, QD | Y | S0034 | 22527 | .5 | MG | CAPSULE | QD | ||||
93423104 | 9342310 | 2 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Unknown | 1000 MG, QD | U | 0 | 1000 | MG | TABLET | QD | |||||
93423104 | 9342310 | 3 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Unknown | 40 MG, QD | U | 0 | 40 | MG | TABLET | QD | |||||
93423104 | 9342310 | 4 | C | TOVIAZ | FESOTERODINE FUMARATE | 1 | Unknown | 8 MG, QD | U | 0 | 8 | MG | TABLET | QD | |||||
93423104 | 9342310 | 5 | C | PREGABALIN. | PREGABALIN | 1 | Oral | 300 MG, QD | U | 0 | 300 | MG | TABLET | QD | |||||
93423104 | 9342310 | 6 | C | BACLOFEN. | BACLOFEN | 1 | Unknown | 10 MG, QD | U | 0 | 10 | MG | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
93423104 | 9342310 | 1 | Relapsing-remitting multiple sclerosis |
93423104 | 9342310 | 2 | Product used for unknown indication |
93423104 | 9342310 | 3 | Product used for unknown indication |
93423104 | 9342310 | 4 | Product used for unknown indication |
93423104 | 9342310 | 5 | Product used for unknown indication |
93423104 | 9342310 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
93423104 | 9342310 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
93423104 | 9342310 | Blood pressure decreased | |
93423104 | 9342310 | Burning sensation | |
93423104 | 9342310 | Dizziness | |
93423104 | 9342310 | Headache | |
93423104 | 9342310 | Hypoaesthesia | |
93423104 | 9342310 | Pain in extremity |
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 |
---|---|---|---|---|---|---|
93423104 | 9342310 | 1 | 20130530 | 0 |