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
124682435 12468243 5 F 20160525 20160816 20160615 20160819 PER US-TAKEDA-2016MPI005303 TAKEDA 88.67 YR M Y 0.00000 20160819 MD US US

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
124682435 12468243 1 PS NINLARO IXAZOMIB 1 Oral 3 MG, UNK U 208462 3 MG CAPSULE
124682435 12468243 2 SS NINLARO IXAZOMIB 1 Oral 4 MG, UNK U 208462 4 MG CAPSULE
124682435 12468243 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Unknown UNK U 0
124682435 12468243 4 C REVLIMID LENALIDOMIDE 1 5 MG, UNK U 0 5 MG CAPSULE
124682435 12468243 5 C ACYCLOVIR /00587301/ ACYCLOVIR 1 U 0
124682435 12468243 6 C FLUCONAZOLE. FLUCONAZOLE 1 U 0
124682435 12468243 7 C SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 U 0
124682435 12468243 8 C PROMETHAZINE HCL PROMETHAZINE HYDROCHLORIDE 1 U 0
124682435 12468243 9 C ZOLPIDEM TARTATE ZOLPIDEM TARTRATE 1 U 0
124682435 12468243 10 C MECLIZINE HCL MECLIZINE HYDROCHLORIDE 1 U 0
124682435 12468243 11 C TAMSULOSIN HCL TAMSULOSIN 1 U 0
124682435 12468243 12 C ASPIRIN /00002701/ ASPIRIN 1 U 0
124682435 12468243 13 C PANTOPRAZOLE SODIUM. PANTOPRAZOLE SODIUM 1 U 0
124682435 12468243 14 C VITAMIN D3 CHOLECALCIFEROL 1 U 0
124682435 12468243 15 C VITAMIN D2 ERGOCALCIFEROL 1 U 0
124682435 12468243 16 C TYLENOL ACETAMINOPHEN 1 U 0
124682435 12468243 17 C CALCIUM CALCIUM 1 U 0
124682435 12468243 18 C ZOMETA ZOLEDRONIC ACID 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124682435 12468243 1 Plasma cell myeloma
124682435 12468243 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124682435 12468243 Decreased appetite
124682435 12468243 Diarrhoea
124682435 12468243 Frequent bowel movements
124682435 12468243 Full blood count decreased
124682435 12468243 Gastrointestinal stoma complication
124682435 12468243 Lethargy
124682435 12468243 Liver function test increased
124682435 12468243 Skin discolouration

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
124682435 12468243 1 20160518 0