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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127456411 | 12745641 | 1 | I | 20160513 | 20160907 | 20160915 | 20160915 | EXP | GB-ABBVIE-16P-167-1727923-00 | ABBVIE | 65.00 | YR | F | Y | 101.00000 | KG | 20160915 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127456411 | 12745641 | 1 | PS | CLARITHROMYCIN. | CLARITHROMYCIN | 1 | Unknown | U | UNKNOWN | 50662 | TABLET | ||||||||
127456411 | 12745641 | 2 | C | BENDROFLUMETHIAZIDE | BENDROFLUMETHIAZIDE | 1 | 1 AD EACH MORNING | 0 | QD | ||||||||||
127456411 | 12745641 | 3 | C | BETAMETHASONE VALERATE. | BETAMETHASONE VALERATE | 1 | 0 | 1 | DF | BID | |||||||||
127456411 | 12745641 | 4 | C | LERCANIDIPINE HYDROCHLORIDE | LERCANIDIPINE HYDROCHLORIDE | 1 | 0 | 1 | DF | QD | |||||||||
127456411 | 12745641 | 5 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | 0 | 1 | DF | BID | |||||||||
127456411 | 12745641 | 6 | C | RAMIPRIL. | RAMIPRIL | 1 | 0 | 1 | DF | QD | |||||||||
127456411 | 12745641 | 7 | C | SIMVASTATIN. | SIMVASTATIN | 1 | 1 AD NOCTE | 0 | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127456411 | 12745641 | 1 | Product used for unknown indication |
127456411 | 12745641 | 2 | Product used for unknown indication |
127456411 | 12745641 | 3 | Product used for unknown indication |
127456411 | 12745641 | 4 | Product used for unknown indication |
127456411 | 12745641 | 5 | Product used for unknown indication |
127456411 | 12745641 | 6 | Product used for unknown indication |
127456411 | 12745641 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127456411 | 12745641 | OT |
127456411 | 12745641 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127456411 | 12745641 | Burning sensation | |
127456411 | 12745641 | Rash |
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 |
---|---|---|---|---|---|---|
127456411 | 12745641 | 1 | 20160513 | 0 | ||
127456411 | 12745641 | 2 | 20150618 | 0 | ||
127456411 | 12745641 | 3 | 20160622 | 20160707 | 0 | |
127456411 | 12745641 | 4 | 20150618 | 0 | ||
127456411 | 12745641 | 5 | 20150618 | 0 | ||
127456411 | 12745641 | 6 | 20150618 | 0 | ||
127456411 | 12745641 | 7 | 20150618 | 0 |