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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125565584 | 12556558 | 4 | F | 20160916 | 20160714 | 20160919 | EXP | US-PFIZER INC-2016332049 | PFIZER | HOFFMANN, M.. ACUTE BENZODIAZEPINE TOXICITY EXACERBATED BY CONCOMITANT ORAL OLANZAPINE. JOURNAL OF COMMUNITY AND SUPPORTIVE ONCOLOGY. 2016;14 (4):178-179 | 61.00 | YR | F | Y | 0.00000 | 20160919 | MD | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125565584 | 12556558 | 1 | PS | LORAZEPAM. | LORAZEPAM | 1 | Intravenous (not otherwise specified) | 1 MG, UNK, AT ABOUT 3:45 PM | U | 74243 | 1 | MG | |||||||
| 125565584 | 12556558 | 2 | I | LORAZEPAM. | LORAZEPAM | 1 | UNK | U | 74243 | ||||||||||
| 125565584 | 12556558 | 3 | I | LORAZEPAM. | LORAZEPAM | 1 | Oral | 1 MG, UNK, AT 1:00 PM | U | 0 | 1 | MG | |||||||
| 125565584 | 12556558 | 4 | I | LORAZEPAM. | LORAZEPAM | 1 | U | 0 | |||||||||||
| 125565584 | 12556558 | 5 | I | OLANZAPINE. | OLANZAPINE | 1 | Oral | 10 MG, UNK, AT 3:15 PM | U | 0 | 10 | MG | |||||||
| 125565584 | 12556558 | 6 | I | OLANZAPINE. | OLANZAPINE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125565584 | 12556558 | 1 | Nausea |
| 125565584 | 12556558 | 2 | Anxiety |
| 125565584 | 12556558 | 3 | Nausea |
| 125565584 | 12556558 | 4 | Anxiety |
| 125565584 | 12556558 | 5 | Nausea |
| 125565584 | 12556558 | 6 | Vomiting |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125565584 | 12556558 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125565584 | 12556558 | Drug interaction | |
| 125565584 | 12556558 | Hypotension | |
| 125565584 | 12556558 | Intentional product use issue | |
| 125565584 | 12556558 | Post-injection delirium sedation syndrome | |
| 125565584 | 12556558 | Respiratory depression |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |