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
114728687 11472868 7 F 20150313 20160725 20150908 20160809 EXP CA-VALIDUS PHARMACEUTICALS LLC-CA-2015VAL000557 VALIDUS 0.00 Y 0.00000 20160809 CN 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
114728687 11472868 1 PS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 100 MG, BID U 17963 100 MG
114728687 11472868 2 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Subcutaneous 200 ?G, BID (TO CONTINUE 2 WEEKS) 0 200 UG
114728687 11472868 3 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Intramuscular 20 MG, QMO (EVERY 4 WEEKS) SANDOSTATIN LAR U 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114728687 11472868 1 Product used for unknown indication
114728687 11472868 2 Neuroendocrine tumour
114728687 11472868 3 Neuroendocrine tumour

Outcome of event

Event ID CASEID OUTC COD
114728687 11472868 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114728687 11472868 Blood glucose increased
114728687 11472868 Blood pressure increased
114728687 11472868 Blood pressure systolic increased
114728687 11472868 Heart rate decreased
114728687 11472868 Nervousness
114728687 11472868 Respiratory rate 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
114728687 11472868 2 201502 2015 0
114728687 11472868 3 20150313 0