The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6524176 7235368 I 6524176-5 20091221 20091231 EXP US-GENENTECH-296210 GNEFDAAERSPRD Y 20091231 MD UNITED KINGDOM

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6524176 1012889289 PS RITUXAN 1 UNKNOWN 375 MG/M2, Q4W NOT REPORTED
6524176 1012889290 SS BORTEZOMIB 1 UNKNOWN 1.3 MG/M2, UNK NOT REPORTED

Indications of drugs used

Event ID DRUG SEQ INDI PT
6524176 1012889289 NON-HODGKIN'S LYMPHOMA
6524176 1012889290 LYMPHOMA

Outcome of event

Event ID OUTC COD
6524176 DE
6524176 OT

Reactions reported

Event ID PT
6524176 ABDOMINAL PAIN
6524176 DECREASED APPETITE
6524176 DIARRHOEA
6524176 DYSPNOEA
6524176 FATIGUE
6524176 HEADACHE
6524176 METABOLIC ACIDOSIS
6524176 MULTI-ORGAN FAILURE
6524176 NAUSEA
6524176 NEUROPATHY PERIPHERAL
6524176 NEUTROPENIA
6524176 RESPIRATORY FAILURE
6524176 SEPSIS
6524176 SEPTIC SHOCK
6524176 THROMBOCYTOPENIA
6524176 VOMITING

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found