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
126473751 12647375 1 I 20160612 20160805 20160812 20160812 EXP PHEH2016US019800 NOVARTIS 66.65 YR F Y 0.00000 20160812 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
126473751 12647375 1 PS ZOMETA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 4MG/5ML U 21223
126473751 12647375 2 SS REVLIMID LENALIDOMIDE 1 Oral 15 MG, (15 MG, 21-2) A2104A 0 15 MG CAPSULE
126473751 12647375 3 C ASPIRIN /00346701/ ASCORBIC ACIDASPIRIN 1 Unknown UNK MG, UNK U 0
126473751 12647375 4 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown UNK U 0
126473751 12647375 5 C GLIMEPIRIDE. GLIMEPIRIDE 1 Unknown 1.5 MG, UNK U 0 1.5 MG
126473751 12647375 6 C LISINOPRIL. LISINOPRIL 1 Unknown 20 TO 12.5 MG U 0 20 MG
126473751 12647375 7 C HYDROCODONE HYDROCODONE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126473751 12647375 1 Bone disorder
126473751 12647375 2 Plasma cell myeloma
126473751 12647375 3 Cardiac disorder
126473751 12647375 4 Plasma cell myeloma
126473751 12647375 5 Diabetes mellitus
126473751 12647375 6 Hypertension
126473751 12647375 7 Pain

Outcome of event

Event ID CASEID OUTC COD
126473751 12647375 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126473751 12647375 Burning sensation
126473751 12647375 Fatigue
126473751 12647375 Neuropathy peripheral
126473751 12647375 Pain

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
126473751 12647375 2 20160610 0