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
126433011 12643301 1 I 20160801 20160811 20160811 PER PHEH2016US019414 NOVARTIS 0.00 F Y 0.00000 20160811 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
126433011 12643301 1 PS RECLAST ZOLEDRONIC ACID 1 Intravenous drip 21817
126433011 12643301 2 C CALCIUM CALCIUM 1 Oral U 0
126433011 12643301 3 C TYLENOL ACETAMINOPHEN 1 Oral UNK, PRN U 0
126433011 12643301 4 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 Oral UNK, PRN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126433011 12643301 1 Osteoporosis
126433011 12643301 2 Product used for unknown indication
126433011 12643301 3 Product used for unknown indication
126433011 12643301 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126433011 12643301 Abdominal pain
126433011 12643301 Fatigue
126433011 12643301 Headache
126433011 12643301 Pain
126433011 12643301 Temperature intolerance

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
126433011 12643301 1 20160602 0