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
126059112 12605911 2 F 20160615 20160810 20160729 20160817 EXP US-AMGEN-USASL2016095249 AMGEN 61.00 YR A F Y 61.00000 KG 20160817 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
126059112 12605911 1 PS PROLIA DENOSUMAB 1 Unknown UNK 125320 SOLUTION FOR INJECTION
126059112 12605911 2 C PROZAC FLUOXETINE HYDROCHLORIDE 1 UNK 0
126059112 12605911 3 C ZORVOLEX DICLOFENAC 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126059112 12605911 1 Osteoporosis postmenopausal

Outcome of event

Event ID CASEID OUTC COD
126059112 12605911 OT
126059112 12605911 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126059112 12605911 Anal incontinence
126059112 12605911 Asthenia
126059112 12605911 Bone pain
126059112 12605911 Death
126059112 12605911 Infection
126059112 12605911 Malaise
126059112 12605911 Mobility decreased
126059112 12605911 Nausea
126059112 12605911 Pain

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found