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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117349841 | 11734984 | 1 | I | 20141113 | 20151113 | 20151113 | EXP | FR-ASTRAZENECA-2015SF10154 | ASTRAZENECA | 44.00 | YR | M | Y | 0.00000 | 20151113 | MD | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117349841 | 11734984 | 1 | PS | XEROQUEL | QUETIAPINE FUMARATE | 1 | Oral | 22047 | 300 | MG | PROLONGED-RELEASE TABLET | QD | |||||||
| 117349841 | 11734984 | 2 | I | METHADONE | METHADONE HYDROCHLORIDE | 1 | Unknown | 0 | |||||||||||
| 117349841 | 11734984 | 3 | I | METHADONE | METHADONE HYDROCHLORIDE | 1 | Unknown | 0 | 100 | MG | |||||||||
| 117349841 | 11734984 | 4 | I | METHADONE | METHADONE HYDROCHLORIDE | 1 | Unknown | 0 | 50 | MG |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117349841 | 11734984 | HO |
| 117349841 | 11734984 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117349841 | 11734984 | Altered state of consciousness | |
| 117349841 | 11734984 | Drug interaction | |
| 117349841 | 11734984 | Miosis | |
| 117349841 | 11734984 | Respiratory depression | |
| 117349841 | 11734984 | Seizure |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |