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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8136094 | 8094842 | F | 8136094-X | 20110709 | 20110815 | 20120214 | EXP | US-TYCO HEALTHCARE/MALLINCKRODT-T201101395 | COVIDIEN | 59 | YR | F | Y | 20120214 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8136094 | 1018859327 | C | FENTANYL | 1 | 50 UG/HR, Q 72 HOURS | ||||||
8136094 | 1018859330 | C | ANTIHYPERTENSIVES | 2 | UNK | ||||||
8136094 | 1018859329 | C | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | 1 | ORAL | 10 MG, TOOK ONE | |||||
8136094 | 1018859331 | C | CHOLESTEROL- AND TRIGLYCERIDE REDUCERS | 2 | UNK | ||||||
8136094 | 1018859328 | C | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | 1 | ORAL | 5/325 MG TABLET, BID | |||||
8136094 | 1018859332 | C | ALLERGY MEDICATION | 2 | UNK | ||||||
8136094 | 1018859326 | PS | FENTANYL-100 | 1 | 50 UG/HR, Q 72 HOURS | 5031790 | 077154 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8136094 | 1018859328 | PAIN |
8136094 | 1018859326 | PAIN |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
8136094 | DRUG EFFECT DECREASED |
8136094 | INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION |
8136094 | DRUG INEFFECTIVE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
8136094 | 1018859327 | 20110709 | |||
8136094 | 1018859329 | 20110709 | 20110709 | 1 | DAY |
8136094 | 1018859326 | 20110709 |