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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126683411 | 12668341 | 1 | I | 20140101 | 20160812 | 20160819 | 20160819 | EXP | GB-MHRA-EYC 00143537 | PHHY2016GB111492 | SANDOZ | 41.00 | YR | F | Y | 69.85000 | KG | 20160819 | OT | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126683411 | 12668341 | 1 | PS | TOPIRAMATE. | TOPIRAMATE | 1 | Oral | Y | 79206 | ||||||||||
126683411 | 12668341 | 2 | C | AMITRIPTYLINE | AMITRIPTYLINE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126683411 | 12668341 | 1 | Hemiplegic migraine |
126683411 | 12668341 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126683411 | 12668341 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126683411 | 12668341 | Abdominal pain upper | |
126683411 | 12668341 | Decreased appetite | |
126683411 | 12668341 | Food intolerance | |
126683411 | 12668341 | Lethargy | |
126683411 | 12668341 | Palpitations |
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 |
---|---|---|---|---|---|---|
126683411 | 12668341 | 1 | 20130301 | 20140401 | 0 |