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
125520673 12552067 3 F 20160103 20160725 20160713 20160808 EXP IT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-120081 RANBAXY 50.00 YR F Y 0.00000 20160808 OT IT IT

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
125520673 12552067 1 PS Paracetamol ACETAMINOPHEN 1 Oral 1000 MG DAILY Y U 76200 1000 MG
125520673 12552067 2 SS EXPOSE 100 MG EPERISONE HYDROCHLORIDE 1 Oral 100 MG DAILY Y U 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125520673 12552067 1 Myalgia
125520673 12552067 2 Myalgia

Outcome of event

Event ID CASEID OUTC COD
125520673 12552067 OT
125520673 12552067 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125520673 12552067 Drug hypersensitivity
125520673 12552067 Dyspnoea
125520673 12552067 Paraesthesia
125520673 12552067 Urticaria

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
125520673 12552067 1 20160101 20160103 0
125520673 12552067 2 20160101 20160103 0