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
126102161 12610216 1 I 20160721 20160801 20160801 EXP DK-MYLANLABS-2016M1030452 MYLAN 0.00 Y 0.00000 20160731 MD 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
126102161 12610216 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown DOSAGE FORM: UNSPECIFIED U 77042
126102161 12610216 2 I BRENTAN /00310801/ MICONAZOLE 1 Oral UNK U U UNKNOWN 0
126102161 12610216 3 I MAREVAN WARFARIN SODIUM 1 Unknown DOSAGE FORM: UNSPECIFIED U U 0
126102161 12610216 4 I PARACETAMOL ACETAMINOPHEN 1 Unknown DOSAGE FORM: UNSPECIFIED U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126102161 12610216 1 Product used for unknown indication
126102161 12610216 2 Product used for unknown indication
126102161 12610216 3 Product used for unknown indication
126102161 12610216 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126102161 12610216 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126102161 12610216 Diplopia
126102161 12610216 Dizziness
126102161 12610216 Drug interaction
126102161 12610216 Haemorrhage
126102161 12610216 Headache
126102161 12610216 International normalised ratio increased
126102161 12610216 Malaise
126102161 12610216 Nasopharyngitis

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

no results found

Therapies reported

no results found