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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126828312 | 12682831 | 2 | F | 20140101 | 20160812 | 20160825 | 20160825 | EXP | GB-CIPLA LTD.-2016GB17596 | CIPLA | 0.00 | Y | 0.00000 | 20160825 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126828312 | 12682831 | 1 | PS | TOPIRAMATE. | TOPIRAMATE | 1 | Oral | NOT KNOWN | Y | U | 79162 | ||||||||
126828312 | 12682831 | 2 | C | Amitriptyline | AMITRIPTYLINE | 1 | Unknown | UNK | U | U | 0 | ||||||||
126828312 | 12682831 | 3 | C | Steroids NOS | UNSPECIFIED INGREDIENT | 1 | Nasal | UNK | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126828312 | 12682831 | 1 | Hemiplegic migraine |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126828312 | 12682831 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126828312 | 12682831 | Abdominal pain upper | |
126828312 | 12682831 | Decreased appetite | |
126828312 | 12682831 | Food intolerance | |
126828312 | 12682831 | Lethargy | |
126828312 | 12682831 | 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 |
---|---|---|---|---|---|---|
126828312 | 12682831 | 1 | 20130301 | 20140401 | 0 |