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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125885461 | 12588546 | 1 | I | 2016 | 20160705 | 20160725 | 20160725 | PER | US-JNJFOC-20160705010 | JANSSEN | 0.00 | F | Y | 68.04000 | KG | 20160725 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125885461 | 12588546 | 1 | PS | TYLENOL 8 HR ARTHRITIS PAIN | ACETAMINOPHEN | 1 | Oral | N | 1387972 | 19872 | TABLET | ||||||||
125885461 | 12588546 | 2 | SS | TYLENOL 8 HR ARTHRITIS PAIN | ACETAMINOPHEN | 1 | Oral | N | 1387972 | 19872 | 2 | DF | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125885461 | 12588546 | 2 | Pain |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125885461 | 12588546 | Drug effect incomplete | |
125885461 | 12588546 | Inappropriate schedule of drug administration |
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 |
---|---|---|---|---|---|---|
125885461 | 12588546 | 2 | 20160628 | 0 |