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
113719146 11371914 6 F 20140217 20160706 20150812 20160711 EXP PHHY2014CA021135 NOVARTIS 66.95 YR F Y 0.00000 20160712 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
113719146 11371914 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (EVERY 4 WEEKS) U 21008 30 MG /month
113719146 11371914 2 C ACCUPRIL QUINAPRIL HYDROCHLORIDE 1 Unknown 20 MG, QD U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113719146 11371914 1 Neuroendocrine tumour
113719146 11371914 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
113719146 11371914 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113719146 11371914 Alopecia
113719146 11371914 Anxiety
113719146 11371914 Blood glucose increased
113719146 11371914 Blood pressure fluctuation
113719146 11371914 Blood pressure increased
113719146 11371914 Body temperature decreased
113719146 11371914 Headache
113719146 11371914 Heart rate increased
113719146 11371914 Heart rate irregular
113719146 11371914 Hepatic lesion
113719146 11371914 Nervousness
113719146 11371914 Palpitations

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
113719146 11371914 1 20140116 0