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
86983013 8698301 3 F 20160720 20120802 20160724 EXP PHHY2010CA37020 NOVARTIS 0.00 F Y 0.00000 20160724 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
86983013 8698301 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO EVERY 4 WEEKS U 21008 30 MG VIAL /month
86983013 8698301 2 C SENOKOT SENNOSIDES 1 U U 0
86983013 8698301 3 C RANITIDINE. RANITIDINE 1 U U 0
86983013 8698301 4 C DESENEX NOS CLOTRIMAZOLE OR MICONAZOLE NITRATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86983013 8698301 1 Acromegaly

Outcome of event

Event ID CASEID OUTC COD
86983013 8698301 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
86983013 8698301 Blood growth hormone increased
86983013 8698301 Blood pressure decreased
86983013 8698301 Blood pressure systolic increased
86983013 8698301 Goitre
86983013 8698301 Heart rate increased
86983013 8698301 Injection site mass
86983013 8698301 Thyroid cyst

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
86983013 8698301 1 20060119 0
86983013 8698301 4 200910 0