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
125736213 12573621 3 F 20151221 20160811 20160720 20160816 EXP PHHY2016BR098569 NOVARTIS 54.29 YR F Y 63.00000 KG 20160816 MD BR BR

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
125736213 12573621 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, Q12MO 21817 5 MG SOLUTION FOR INJECTION
125736213 12573621 2 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 100 MG, QD (10 YEARS AGO) 0 100 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125736213 12573621 1 Osteoporosis
125736213 12573621 2 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
125736213 12573621 LT
125736213 12573621 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125736213 12573621 Apparent death
125736213 12573621 Arthralgia
125736213 12573621 Dengue fever
125736213 12573621 Erythema
125736213 12573621 Malaise
125736213 12573621 Pain
125736213 12573621 Pain in extremity
125736213 12573621 Pruritus
125736213 12573621 Pyrexia
125736213 12573621 Rash

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
125736213 12573621 1 20151221 0