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
127472181 12747218 1 I 20160107 20160906 20160915 20160915 EXP IT-MINISAL02-373515 IT-MYLANLABS-2016M1038128 MYLAN 0.00 Y 0.00000 20160915 MD 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
127472181 12747218 1 PS BISOPROLOL BISOPROLOL 1 Oral 2.5 MG DAILY U U 75831 2.5 MG QD
127472181 12747218 2 SS COUMADIN WARFARIN SODIUM 1 Oral 2.5 MG DAILY U U 0 2.5 MG QD
127472181 12747218 3 C EUTIROX LEVOTHYROXINE SODIUM 1 UNK 0
127472181 12747218 4 C XANAX ALPRAZOLAM 1 UNK 0
127472181 12747218 5 C LANSOX LANSOPRAZOLE 1 UNK 0
127472181 12747218 6 C FUROSEMIDE. FUROSEMIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127472181 12747218 1 Cardiac failure
127472181 12747218 2 Anticoagulant therapy
127472181 12747218 3 Product used for unknown indication
127472181 12747218 4 Product used for unknown indication
127472181 12747218 5 Product used for unknown indication
127472181 12747218 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127472181 12747218 HO
127472181 12747218 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127472181 12747218 Condition aggravated
127472181 12747218 Congestive cardiomyopathy
127472181 12747218 Hypotension
127472181 12747218 Pleural effusion
127472181 12747218 Pulmonary embolism

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
127472181 12747218 1 20150101 0
127472181 12747218 2 20150101 0