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
127601641 12760164 1 I 20160704 20160912 20160919 20160919 EXP GB-BAUSCH-BL-2016-022620 BAUSCH AND LOMB 84.00 YR M Y 0.00000 20160919 MD GB GB

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
127601641 12760164 1 PS DEXAMETHASONE. DEXAMETHASONE 1 Oral D 40069 20 MG SOLUTION
127601641 12760164 2 SS FARYDAK PANOBINOSTAT 1 Oral D 0 15 MG CAPSULE QD
127601641 12760164 3 SS VELCADE BORTEZOMIB 1 Subcutaneous D 0 1.3 MG
127601641 12760164 4 C ACICLOVIR ACYCLOVIR 1 Oral 0 400 MG BID
127601641 12760164 5 C RANITIDINE. RANITIDINE 1 Oral 0 150 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127601641 12760164 1 Plasma cell myeloma
127601641 12760164 2 Plasma cell myeloma
127601641 12760164 3 Plasma cell myeloma
127601641 12760164 4 Prophylaxis
127601641 12760164 5 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127601641 12760164 DE
127601641 12760164 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127601641 12760164 Acute kidney injury
127601641 12760164 Blood creatinine increased
127601641 12760164 Lethargy
127601641 12760164 Lower respiratory tract infection
127601641 12760164 Lung consolidation
127601641 12760164 Pyrexia

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
127601641 12760164 1 20160609 20160704 0
127601641 12760164 2 20160609 20160704 0
127601641 12760164 3 20160609 20160704 0
127601641 12760164 4 20160609 20160704 0
127601641 12760164 5 20160609 20160704 0