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
125310821 12531082 1 I 20160630 20160706 20160706 EXP PHHY2016BR091810 NOVARTIS 0.00 F Y 45.00000 KG 20160706 CN 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
125310821 12531082 1 PS VOLTAREN DICLOFENAC SODIUM 1 Rectal 5 DF, Q6H N 0 5 DF SUPPOSITORY Q6H
125310821 12531082 2 C PARACETAMOL ACETAMINOPHEN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125310821 12531082 1 Torticollis
125310821 12531082 2 Pain

Outcome of event

Event ID CASEID OUTC COD
125310821 12531082 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125310821 12531082 Arthritis
125310821 12531082 Cough
125310821 12531082 Dengue fever
125310821 12531082 Influenza
125310821 12531082 Joint stiffness
125310821 12531082 Osteoarthritis
125310821 12531082 Pain
125310821 12531082 Spinal pain

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
125310821 12531082 1 2014 0
125310821 12531082 2 20160629 0