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
121609643 12160964 3 F 20160125 20160801 20160308 20160812 EXP BX20160322 FR-VALIDUS PHARMACEUTICALS LLC-FR-2016VAL000373 VALIDUS 64.00 YR M Y 0.00000 20160812 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
121609643 12160964 1 PS FUROSEMIDE. FUROSEMIDE 1 Unknown UNK U UNK 16273
121609643 12160964 2 SS XATRAL ALFUZOSIN 1 Unknown UNK U UNK 0
121609643 12160964 3 SS ERY /00020901/ ERYTHROMYCIN 1 Oral UNK Y UNK 0
121609643 12160964 4 SS LEXOMIL BROMAZEPAM 1 Unknown UNK U UNK 0
121609643 12160964 5 SS PHOSPHONEUROS CALCIUM PHOSPHATE, DIBASIC, ANHYDROUSMAGNESIUM GLYCEROPHOSPHATEPHOSPHORIC ACIDSODIUM PHOSPHATE, DIBASIC 1 Unknown UNK U UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121609643 12160964 1 Product used for unknown indication
121609643 12160964 2 Product used for unknown indication
121609643 12160964 3 Gastrointestinal disorder
121609643 12160964 4 Product used for unknown indication
121609643 12160964 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121609643 12160964 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121609643 12160964 Aplasia

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
121609643 12160964 1 20160119 0
121609643 12160964 2 20160122 0
121609643 12160964 3 20160115 20160119 0
121609643 12160964 4 20160119 0
121609643 12160964 5 20160123 0