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
126072211 12607221 1 I 201605 20160715 20160729 20160729 EXP BX20161109 FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL002347 VALIDUS 82.00 YR F Y 0.00000 20160729 OT FR FR

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
126072211 12607221 1 PS FUROSEMIDE. FUROSEMIDE 1 Oral 250 MG, DAILY UNKNOWN 16273 250 MG TABLET
126072211 12607221 2 SS AMIODARONE HYDROCHLORIDE. AMIODARONE HYDROCHLORIDE 1 Unknown 200 MG, DAILY Y UNKNOWN 0 200 MG
126072211 12607221 3 SS PRISTINAMYCIN PRISTINAMYCIN 1 Oral 2 DF, UNK Y UNKNOWN 0 2 DF
126072211 12607221 4 SS AMOXICILLIN. AMOXICILLIN 1 Oral 1.5 MG, UNK Y UNKNOWN 0 1.5 MG
126072211 12607221 5 C PREVISCAN /00261401/ PENTOXIFYLLINE 1 U 0
126072211 12607221 6 C BISOPROLOL BISOPROLOL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126072211 12607221 1 Cardiac failure
126072211 12607221 2 Atrial flutter
126072211 12607221 3 Erysipelas
126072211 12607221 4 Erysipelas
126072211 12607221 5 Product used for unknown indication
126072211 12607221 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126072211 12607221 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126072211 12607221 Erythema

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
126072211 12607221 1 201604 0
126072211 12607221 2 20160406 0
126072211 12607221 3 20160423 20160429 0
126072211 12607221 4 20160418 20160423 0