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
125243731 12524373 1 I 20140821 20140822 20160704 20160704 EXP PHHY2014CA107264 NOVARTIS 66.33 YR F Y 0.00000 20160704 MD CA CA

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
125243731 12524373 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, EVERY 4 WEEKS 630.689026 MG Y 21008 30 MG SUSPENSION /month
125243731 12524373 2 SS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD Y 0 10 MG QD
125243731 12524373 3 SS SUTENT SUNITINIB MALATE 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125243731 12524373 1 Pancreatic neuroendocrine tumour
125243731 12524373 2 Pancreatic neuroendocrine tumour
125243731 12524373 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125243731 12524373 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125243731 12524373 Abdominal pain upper
125243731 12524373 Arthralgia
125243731 12524373 Blood glucose increased
125243731 12524373 Blood magnesium decreased
125243731 12524373 Blood pressure systolic increased
125243731 12524373 Feeding disorder
125243731 12524373 Feeling abnormal
125243731 12524373 Gait disturbance
125243731 12524373 H1N1 influenza
125243731 12524373 Headache
125243731 12524373 Hepatic neoplasm
125243731 12524373 Hepatic pain
125243731 12524373 Injection site pain
125243731 12524373 Injection site swelling
125243731 12524373 Ligament sprain
125243731 12524373 Malaise
125243731 12524373 Musculoskeletal pain
125243731 12524373 Pain
125243731 12524373 Pertussis
125243731 12524373 Stomatitis
125243731 12524373 Tumour pain
125243731 12524373 Weight decreased
125243731 12524373 Weight increased

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
125243731 12524373 1 20140722 20160504 0
125243731 12524373 2 20150305 2016 0