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 |