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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126002251 | 12600225 | 1 | I | 20150818 | 20150819 | 20160727 | 20160727 | PER | US-ENDO PHARMACEUTICALS INC.-2015-002516 | ENDO | 60.71 | YR | F | Y | 60.84000 | KG | 20160727 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126002251 | 12600225 | 1 | PS | PROMETHAZINE HYDROCHLORIDE TABLETS 25MG | PROMETHAZINE HYDROCHLORIDE | 1 | Oral | UNKNOWN | 40622 | 25 | MG | TABLETS | |||||||
126002251 | 12600225 | 2 | SS | PROMETHAZINE HYDROCHLORIDE TABLETS 25MG | PROMETHAZINE HYDROCHLORIDE | 1 | UNKNOWN | 40622 | |||||||||||
126002251 | 12600225 | 3 | C | OXYCODONE HYDROCHLORIDE. | OXYCODONE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126002251 | 12600225 | 1 | Nausea |
126002251 | 12600225 | 2 | Vomiting |
126002251 | 12600225 | 3 | Pain |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126002251 | 12600225 | Constipation | |
126002251 | 12600225 | Drug ineffective | |
126002251 | 12600225 | Hyperhidrosis | |
126002251 | 12600225 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
126002251 | 12600225 | 1 | 2014 | 0 |