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
126763662 12676366 2 F 201601 20160902 20160823 20160907 EXP PHHY2016MX115160 NOVARTIS 58.95 YR F Y 0.00000 20160907 CN COUNTRY NOT SPECIFIED MX

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
126763662 12676366 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, Q12MO 21817 5 MG SOLUTION FOR INJECTION
126763662 12676366 2 SS ACLASTA ZOLEDRONIC ACID 1 21817 SOLUTION FOR INJECTION
126763662 12676366 3 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 2 DF, QD (SINCE 6 MONTHS AGO) 0 2 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126763662 12676366 1 Osteoporosis
126763662 12676366 2 Osteopenia
126763662 12676366 3 Systemic lupus erythematosus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126763662 12676366 Arthralgia
126763662 12676366 Inflammation
126763662 12676366 Tendonitis

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
126763662 12676366 1 201508 0