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
125987541 12598754 1 I 20160513 20160713 20160727 20160727 EXP US-PERNIX THERAPEUTICS-2016PT000150 PERNIX 0.00 Y 0.00000 20160726 CN 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
125987541 12598754 1 PS HYDROCODONE HYDROCODONE 1 Unknown UNK UNK, ONCE Y U UNKNOWN 202880 TABLET 1X
125987541 12598754 2 SS EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, DAILY UNKNOWN 0 75 MG QD
125987541 12598754 3 SS OXYCODONE W/APAP ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 Oral 5/325 TABLET, Q 4-6 HOURS PRN Y U UNKNOWN 0
125987541 12598754 4 C SIMVASTATIN. SIMVASTATIN 1 Unknown 20 MG, UNKNOWN UNKNOWN 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125987541 12598754 1 Pain
125987541 12598754 2 Depression
125987541 12598754 3 Pain
125987541 12598754 4 Blood cholesterol abnormal

Outcome of event

Event ID CASEID OUTC COD
125987541 12598754 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125987541 12598754 Breast cancer
125987541 12598754 Drug ineffective
125987541 12598754 Serotonin syndrome

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
125987541 12598754 1 20160513 20160513 0
125987541 12598754 2 2014 0
125987541 12598754 3 20160513 20160513 0
125987541 12598754 4 201601 0