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
116878876 11687887 6 F 2015 20160718 20151030 20160722 EXP PHHY2015CA136669 NOVARTIS 74.01 YR F Y 0.00000 20160722 CN COUNTRY NOT SPECIFIED 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
116878876 11687887 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (EVERY 4 WEEKS) U 21008 30 MG /month
116878876 11687887 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QW3 U 21008 30 MG TIW
116878876 11687887 3 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Subcutaneous 50 UG, ONCE/SINGLE TEST DOSE 50 UG 0 50 UG 1X
116878876 11687887 4 C PULMICORT TURBUHALER BUDESONIDE 1 Unknown U 0
116878876 11687887 5 C TECTA PANTOPRAZOLE MAGNESIUM 1 Unknown U 0
116878876 11687887 6 C MACROBID NITROFURANTOINNITROFURANTOIN MONOHYDRATE 1 Unknown U 0
116878876 11687887 7 C FAMOTIDINE. FAMOTIDINE 1 Unknown U 0
116878876 11687887 8 C PREDNISONE. PREDNISONE 1 Unknown U 0
116878876 11687887 9 C ATIVAN LORAZEPAM 1 Unknown U 0
116878876 11687887 10 C DOMPERIDONE DOMPERIDONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116878876 11687887 1 Neuroendocrine tumour
116878876 11687887 3 Neuroendocrine tumour
116878876 11687887 4 Product used for unknown indication
116878876 11687887 5 Product used for unknown indication
116878876 11687887 6 Product used for unknown indication
116878876 11687887 7 Product used for unknown indication
116878876 11687887 8 Product used for unknown indication
116878876 11687887 9 Product used for unknown indication
116878876 11687887 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
116878876 11687887 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116878876 11687887 Abdominal pain upper
116878876 11687887 Blood pressure increased
116878876 11687887 Concussion
116878876 11687887 Contrast media reaction
116878876 11687887 Dyspnoea
116878876 11687887 Facial bones fracture
116878876 11687887 Fall
116878876 11687887 Flatulence
116878876 11687887 Fracture
116878876 11687887 Headache
116878876 11687887 Hypophagia
116878876 11687887 Impaired healing
116878876 11687887 Inappropriate schedule of drug administration
116878876 11687887 Injury
116878876 11687887 Ligament injury
116878876 11687887 Lip injury
116878876 11687887 Malaise
116878876 11687887 Myalgia
116878876 11687887 Nausea
116878876 11687887 Oral pain
116878876 11687887 Pain
116878876 11687887 Somnolence
116878876 11687887 Tooth injury
116878876 11687887 Vomiting

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
116878876 11687887 1 20151113 0
116878876 11687887 3 20151015 20151015 0