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
126062701 12606270 1 I 20160721 20160729 20160729 EXP DK-WATSON-2016-16658 WATSON 75.00 YR M Y 0.00000 20160729 CN 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
126062701 12606270 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown UNK UNCONFIRMED 77034 UNK
126062701 12606270 2 I Paracetamol (Unknown) ACETAMINOPHEN 1 Unknown UNK UNCONFIRMED 0 UNK
126062701 12606270 3 I BRENTAN /00310801/ MICONAZOLE 1 Oral UNK U 0 GEL
126062701 12606270 4 I MAREVAN WARFARIN SODIUM 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126062701 12606270 1 Product used for unknown indication
126062701 12606270 2 Product used for unknown indication
126062701 12606270 3 Product used for unknown indication
126062701 12606270 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126062701 12606270 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126062701 12606270 Diplopia
126062701 12606270 Dizziness
126062701 12606270 Drug interaction
126062701 12606270 Haemorrhage
126062701 12606270 Headache
126062701 12606270 International normalised ratio increased
126062701 12606270 Malaise
126062701 12606270 Nasopharyngitis

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

no results found

Therapies reported

no results found