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
126451132 12645113 2 F 2006 20160819 20160811 20160825 EXP PHHY2016BR103398 NOVARTIS 0.00 F Y 60.00000 KG 20160825 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
126451132 12645113 1 SS VOLTAREN DICLOFENAC SODIUM 1 Rectal 1 DF (50 MG), QD Y U 0 1 DF SUPPOSITORY QD
126451132 12645113 2 SS VOLTAREN DICLOFENAC SODIUM 1 Y U 0 SUPPOSITORY
126451132 12645113 3 SS VOLTAREN DICLOFENAC SODIUM 1 Y U 0 SUPPOSITORY
126451132 12645113 4 PS VOLTAREN DICLOFENAC SODIUM 1 Unknown UNK U 19201 TABLET
126451132 12645113 5 SS VOLTAREN DICLOFENAC SODIUM 1 Endocervical UNK U 19201 TABLET
126451132 12645113 6 SS VOLTAREN DICLOFENAC SODIUM 1 Unknown UNK U 19201 TABLET
126451132 12645113 7 SS ARCOXIA ETORICOXIB 1 Unknown U 0
126451132 12645113 8 C PIROXICAM. PIROXICAM 1 Unknown 20 MG, UNK U 0 20 MG
126451132 12645113 9 C NIMESULIDE NIMESULIDE 1 Unknown U 0
126451132 12645113 10 C OPTAMAX 2 Unknown U 0
126451132 12645113 11 C CATAFLAM DICLOFENAC POTASSIUM 1 Unknown 50 MG, UNK U 0 50 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126451132 12645113 1 Chest pain
126451132 12645113 2 Spinal pain
126451132 12645113 3 Neck pain
126451132 12645113 4 Chest pain
126451132 12645113 5 Spinal pain
126451132 12645113 6 Neck pain
126451132 12645113 7 Product used for unknown indication
126451132 12645113 8 Product used for unknown indication
126451132 12645113 9 Product used for unknown indication
126451132 12645113 10 Product used for unknown indication
126451132 12645113 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126451132 12645113 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126451132 12645113 Cold sweat
126451132 12645113 Dizziness
126451132 12645113 Fall
126451132 12645113 Hypotension
126451132 12645113 Sluggishness
126451132 12645113 Tremor
126451132 12645113 Vomiting

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
126451132 12645113 1 1999 2014 0
126451132 12645113 4 2006 0
126451132 12645113 5 2007 0
126451132 12645113 6 2013 0