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
126107421 12610742 1 I 20151201 20160726 20160801 20160801 EXP IT-PFIZER INC-2016363960 PFIZER 49.00 YR M Y 0.00000 20160801 PH 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
126107421 12610742 1 PS ELETRIPTAN HBR ELETRIPTAN HYDROBROMIDE 1 Oral 400 MG, MONTHLY Y 21016 400 MG /month
126107421 12610742 2 SS PARACETAMOL ACETAMINOPHEN 1 Oral 20 G, MONTHLY U 0 20 G /month
126107421 12610742 3 SS RIVOTRIL CLONAZEPAM 1 Oral 60 GTT, DAILY Y 0 60 GTT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126107421 12610742 1 Headache
126107421 12610742 2 Headache

Outcome of event

Event ID CASEID OUTC COD
126107421 12610742 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126107421 12610742 Blood creatine phosphokinase increased
126107421 12610742 Drug abuse
126107421 12610742 Product use issue

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
126107421 12610742 1 20151201 20160704 0
126107421 12610742 2 20151201 20160704 0
126107421 12610742 3 20151201 20160704 0