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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
113179112 | 11317911 | 2 | F | 20160817 | 20150728 | 20160819 | PER | US-PFIZER INC-2015241452 | PFIZER | 58.00 | YR | M | Y | 87.00000 | KG | 20160819 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
113179112 | 11317911 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Oral | 600 MG, 3X/DAY | U | 0 | 600 | MG | TID | ||||||
113179112 | 11317911 | 2 | SS | IBUPROFEN. | IBUPROFEN | 1 | 800 MG, 2X/DAY | U | 0 | 800 | MG | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
113179112 | 11317911 | 1 | Pain |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
113179112 | 11317911 | Condition aggravated | |
113179112 | 11317911 | Drug ineffective | |
113179112 | 11317911 | Overdose | |
113179112 | 11317911 | 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 |
---|---|---|---|---|---|---|
113179112 | 11317911 | 1 | 20150704 | 0 |