Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7229317 | 8153900 | I | 7229317-2 | 20101230 | 20110117 | EXP | US-PAR PHARMACEUTICAL, INC-2011SCPR002475 | PARPHARMAP | 42 | YR | F | Y | 20110117 | MD | UNITED STATES |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
7229317 | 1015537975 | C | DRUG UNKNOWN | 2 | ORAL | UNK | |||||
7229317 | 1015537973 | PS | PROPOXYPHENE HYDROCHLORIDE | 1 | ORAL | UNK | 80269 | ||||
7229317 | 1015537974 | SS | ACETAMINOPHEN | 1 | ORAL | UNK |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7229317 | 1015537975 | PRODUCT USED FOR UNKNOWN INDICATION |
7229317 | 1015537973 | PRODUCT USED FOR UNKNOWN INDICATION |
7229317 | 1015537974 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
7229317 | DE |
Reactions reported
Event ID | PT |
---|---|
7229317 | COMPLETED SUICIDE |
7229317 | RESPIRATORY ARREST |
7229317 | DEATH |
7229317 | CARDIO-RESPIRATORY ARREST |
7229317 | CARDIAC ARREST |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |