The Safety Rates Drug Report

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Drug     Injury     Quarter    

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