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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 110546962 | 11054696 | 2 | F | 20040927 | 20150422 | 20160831 | EXP | US-JNJFOC-2004071481 | JANSSEN | WATSON WA, LITOVITZ TL, KLEIN-SCHWARTZ W, RODGERS GC, YOUNISS J, REID N, ET AL. 2003 ANNUAL REPORT OF THE AMERICAN ASSOCIATION OF POISON CONTROL CENTERS TOXIC EXPOSURE SURVEILLANCE SYSTEM. AMERICAN JOURNAL OF EMERGENCY MEDICINE SEP-2004;27/5. | 46.00 | YR | A | M | Y | 0.00000 | 20160831 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 110546962 | 11054696 | 1 | PS | DIPHENHYDRAMINE. | DIPHENHYDRAMINE | 1 | Oral | N | UNK | 999999 | UNSPECIFIED | ||||||||
| 110546962 | 11054696 | 2 | SS | DIPHENHYDRAMINE. | DIPHENHYDRAMINE | 1 | Oral | DAILY DOSE TEXT: UNSPECIFIED | N | UNK | 5845 | UNSPECIFIED | |||||||
| 110546962 | 11054696 | 3 | SS | IBUPROFEN. | IBUPROFEN | 1 | Oral | DAILY DOSE TEXT: UNSPECIFIED | N | UNK | 0 | UNSPECIFIED | |||||||
| 110546962 | 11054696 | 4 | SS | CHLORZOXAZONE. | CHLORZOXAZONE | 1 | Oral | N | UNK | 11300 | TABLETS | ||||||||
| 110546962 | 11054696 | 5 | SS | METHYLPHENIDATE. | METHYLPHENIDATE | 1 | Oral | N | UNK | 21121 | UNSPECIFIED | ||||||||
| 110546962 | 11054696 | 6 | SS | HALOPERIDOL. | HALOPERIDOL | 1 | Oral | N | UNK | 15923 | UNSPECIFIED | ||||||||
| 110546962 | 11054696 | 7 | SS | CYCLOBENZAPRINE | CYCLOBENZAPRINE | 1 | Oral | DAILY DOSE TEXT: UNSPECIFIED | N | UNK | 0 | TABLETS | |||||||
| 110546962 | 11054696 | 8 | SS | CEFALEXIN | CEPHALEXIN | 1 | Oral | DAILY DOSE TEXT: UNSPECIFIED | N | UNK | 0 | UNSPECIFIED | |||||||
| 110546962 | 11054696 | 9 | SS | NAPROXEN. | NAPROXEN | 1 | Oral | DAILY DOSE TEXT: UNSPECIFIED | N | UNK | 0 | UNSPECIFIED | |||||||
| 110546962 | 11054696 | 10 | SS | ETHANOL | ALCOHOL | 1 | Oral | DAILY DOSE TEXT: UNSPECIFIED | N | UNK | 0 | UNSPECIFIED |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 110546962 | 11054696 | 2 | Suicide attempt |
| 110546962 | 11054696 | 3 | Suicide attempt |
| 110546962 | 11054696 | 4 | Suicide attempt |
| 110546962 | 11054696 | 5 | Suicide attempt |
| 110546962 | 11054696 | 6 | Suicide attempt |
| 110546962 | 11054696 | 7 | Suicide attempt |
| 110546962 | 11054696 | 8 | Suicide attempt |
| 110546962 | 11054696 | 9 | Suicide attempt |
| 110546962 | 11054696 | 10 | Suicide attempt |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 110546962 | 11054696 | HO |
| 110546962 | 11054696 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 110546962 | 11054696 | Blood disorder | |
| 110546962 | 11054696 | Completed suicide | |
| 110546962 | 11054696 | Electrocardiogram QRS complex shortened | |
| 110546962 | 11054696 | Intentional overdose | |
| 110546962 | 11054696 | Intentional product misuse | |
| 110546962 | 11054696 | Respiratory arrest | |
| 110546962 | 11054696 | Stupor |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |