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
127851701 12785170 1 I 20160921 20160927 20160927 PER PHEH2016US024272 NOVARTIS 0.00 F Y 0.00000 20160927 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
127851701 12785170 1 PS RECLAST ZOLEDRONIC ACID 1 Unknown D 21817
127851701 12785170 2 C MULTIVITAMINS VITAMINS 1 Unknown U 0
127851701 12785170 3 C VITA-B 2 Unknown U 0
127851701 12785170 4 C ENDOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 Unknown AS NEEDED U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127851701 12785170 1 Product used for unknown indication
127851701 12785170 2 Product used for unknown indication
127851701 12785170 3 Product used for unknown indication
127851701 12785170 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127851701 12785170 Arthralgia
127851701 12785170 Back pain
127851701 12785170 Bone pain
127851701 12785170 Headache
127851701 12785170 Nausea
127851701 12785170 Pain
127851701 12785170 Pain in extremity
127851701 12785170 Vomiting

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

no results found

Therapies reported

no results found