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
126003291 12600329 1 I 20160721 20160727 20160727 EXP PHHY2016DK100538 SANDOZ 75.00 YR M Y 0.00000 20160727 OT DK DK

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
126003291 12600329 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown DOSAGE FORM: UNSPECIFIED U 77040
126003291 12600329 2 I PARACETAMOL ACETAMINOPHEN 1 Unknown U 0
126003291 12600329 3 I BRENTAN//MICONAZOLE MICONAZOLE 1 Oral U UNKNOWN 0 GEL
126003291 12600329 4 I MAREVAN WARFARIN SODIUM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126003291 12600329 1 Product used for unknown indication
126003291 12600329 2 Product used for unknown indication
126003291 12600329 3 Product used for unknown indication
126003291 12600329 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126003291 12600329 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126003291 12600329 Diplopia
126003291 12600329 Dizziness
126003291 12600329 Drug interaction
126003291 12600329 Haemorrhage
126003291 12600329 Headache
126003291 12600329 International normalised ratio increased
126003291 12600329 Malaise
126003291 12600329 Nasopharyngitis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found