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
127393131 12739313 1 I 20160107 20160905 20160913 20160913 EXP PHHY2016IT123773 SANDOZ 72.22 YR F Y 0.00000 20160913 OT IT IT

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
127393131 12739313 1 PS BISOPROLOL BISOPROLOL 1 Oral 2.5 MG, QD 930 MG 75643 2.5 MG QD
127393131 12739313 2 SS COUMADIN WARFARIN SODIUM 1 Oral 2.5 MG, QD 930 MG 0 2.5 MG TABLET QD
127393131 12739313 3 C LANSOX LANSOPRAZOLE 1 Unknown U 0
127393131 12739313 4 C XANAX ALPRAZOLAM 1 Unknown U 0 TABLET
127393131 12739313 5 C EUTIROX LEVOTHYROXINE SODIUM 1 Unknown U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127393131 12739313 1 Cardiac failure
127393131 12739313 2 Anticoagulant therapy
127393131 12739313 3 Product used for unknown indication
127393131 12739313 4 Product used for unknown indication
127393131 12739313 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127393131 12739313 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127393131 12739313 Asthenia
127393131 12739313 Condition aggravated
127393131 12739313 Cough
127393131 12739313 Decreased appetite
127393131 12739313 Dyspnoea
127393131 12739313 Hypotension
127393131 12739313 Pleural effusion

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
127393131 12739313 1 20150101 20160107 0
127393131 12739313 2 20150101 20160107 0