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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126223761 | 12622376 | 1 | I | 20160802 | 20160804 | 20160804 | EXP | AU-ASTRAZENECA-2016SE83648 | ASTRAZENECA | 31.00 | YR | M | Y | 0.00000 | 20160804 | OT | AU | AU |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126223761 | 12622376 | 1 | PS | QUETIAPINE. | QUETIAPINE | 1 | Oral | U | 20639 | TABLET |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126223761 | 12622376 | DE |
126223761 | 12622376 | OT |
126223761 | 12622376 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126223761 | 12622376 | Cardiac arrest | |
126223761 | 12622376 | Depressed level of consciousness | |
126223761 | 12622376 | Overdose | |
126223761 | 12622376 | Respiratory depression | |
126223761 | 12622376 | Seizure |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |