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
126053912 12605391 2 F 20160720 20160802 20160729 20160809 EXP CA-AMGEN-CANSL2016095717 AMGEN 0.00 F Y 0.00000 20160809 CN CA CA

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
126053912 12605391 1 PS PROLIA DENOSUMAB 1 Unknown UNK 125320 SOLUTION FOR INJECTION
126053912 12605391 2 C TRAMCET ACETAMINOPHENTRAMADOL 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126053912 12605391 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126053912 12605391 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126053912 12605391 Activities of daily living impaired
126053912 12605391 Asthenia
126053912 12605391 Fatigue
126053912 12605391 Hyponatraemia
126053912 12605391 Malaise
126053912 12605391 Muscle spasms
126053912 12605391 Muscular weakness
126053912 12605391 Myalgia
126053912 12605391 Pain in extremity
126053912 12605391 Sluggishness

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
126053912 12605391 1 20160720 0