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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126544321 | 12654432 | 1 | I | 20160802 | 20160816 | 20160816 | EXP | US-AUROBINDO-AUR-APL-2016-10321 | AUROBINDO | 0.00 | Y | 0.00000 | 20160816 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126544321 | 12654432 | 1 | PS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Unknown | U | 2147483647 | ORAL LIQUID | |||||||||
126544321 | 12654432 | 2 | SS | Divalproex | DIVALPROEX SODIUM | 1 | Unknown | U | 0 | ||||||||||
126544321 | 12654432 | 3 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126544321 | 12654432 | 1 | Product used for unknown indication |
126544321 | 12654432 | 2 | Product used for unknown indication |
126544321 | 12654432 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126544321 | 12654432 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126544321 | 12654432 | Hepatotoxicity | |
126544321 | 12654432 | Intentional overdose | |
126544321 | 12654432 | Suicide attempt |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |