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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124457932 | 12445793 | 2 | F | 20160515 | 20160613 | 20160608 | 20160725 | PER | US-JNJFOC-20160516207 | JANSSEN | 79.00 | YR | E | F | Y | 70.31000 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124457932 | 12445793 | 1 | PS | TYLENOL 8 HR ARTHRITIS PAIN | ACETAMINOPHEN | 1 | Oral | Y | N | 1390874 | 19872 | TABLET | |||||||
124457932 | 12445793 | 2 | SS | TYLENOL 8 HR ARTHRITIS PAIN | ACETAMINOPHEN | 1 | Oral | MORNING AND EVENING??650MG | Y | N | 1390874 | 19872 | 1 | DF | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124457932 | 12445793 | 2 | Arthralgia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124457932 | 12445793 | Drug ineffective | |
124457932 | 12445793 | Inappropriate schedule of drug administration | |
124457932 | 12445793 | Incorrect dose administered | |
124457932 | 12445793 | Product packaging issue | |
124457932 | 12445793 | Swelling |
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 |
---|---|---|---|---|---|---|
124457932 | 12445793 | 2 | 20160515 | 20160516 | 0 |