The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
125985861 12598586 1 I 20160715 20160720 20160727 20160727 EXP US-PURDUE PHARMA-USA-2016-0132418 PURDUE 35.79 YR F Y 0.00000 20160727 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
125985861 12598586 1 PS DILAUDID HYDROMORPHONE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 2 MG, Q4H PRN UNKNOWN 19034 2 MG INJECTION
125985861 12598586 2 SS ZYVOX LINEZOLID 1 Oral 600 MG, BID UNKNOWN 0 600 MG
125985861 12598586 3 SS VALIUM DIAZEPAM 1 Oral 10 MG, TID UNKNOWN 0 10 MG
125985861 12598586 4 SS SOMA CARISOPRODOL 1 Oral UNK UNKNOWN 0
125985861 12598586 5 SS NEURONTIN GABAPENTIN 1 Oral UNK UNKNOWN 0
125985861 12598586 6 SS PEPCID FAMOTIDINE 1 Oral UNK UNKNOWN 0
125985861 12598586 7 C MS CONTIN MORPHINE SULFATE 1 Oral 30 MG, Q8H UNKNOWN 0 30 MG PROLONGED-RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125985861 12598586 1 Pain
125985861 12598586 2 Infection
125985861 12598586 3 Muscle spasms
125985861 12598586 4 Muscle spasms
125985861 12598586 5 Neuralgia
125985861 12598586 6 Antacid therapy
125985861 12598586 7 Pain

Outcome of event

Event ID CASEID OUTC COD
125985861 12598586 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125985861 12598586 Diarrhoea
125985861 12598586 Discomfort
125985861 12598586 Inappropriate schedule of drug administration
125985861 12598586 Infection

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
125985861 12598586 2 20160711 0