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
72488399 7248839 9 F 2013 20160804 20100119 20160812 EXP PHHY2009CA56003 NOVARTIS 73.44 YR F Y 0.00000 20160812 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
72488399 7248839 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (EVERY 4 WEEKS) Y 21008 30 MG /month
72488399 7248839 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 20 MG, QMO (EVERY 4 WEEKS) Y 21008 20 MG /month
72488399 7248839 3 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (EVERY FOUR WEEKS) Y 21008 30 MG /month
72488399 7248839 4 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 20 MG, QMO (EVERY FOUR WEEKS) Y 21008 20 MG /month
72488399 7248839 5 SS JANUVIA SITAGLIPTIN PHOSPHATE 1 Unknown U 0
72488399 7248839 6 C GLYBURIDE. GLYBURIDE 1 Unknown 5 MG, QD U 0 5 MG QD
72488399 7248839 7 C OXYCONTIN PRN 2 Unknown UNK, PRN U 0
72488399 7248839 8 C ACCUPRIL QUINAPRIL HYDROCHLORIDE 1 Unknown 40 MG, QD U 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
72488399 7248839 1 Neuroendocrine tumour
72488399 7248839 5 Blood glucose abnormal
72488399 7248839 6 Blood glucose abnormal
72488399 7248839 7 Product used for unknown indication
72488399 7248839 8 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
72488399 7248839 OT
72488399 7248839 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
72488399 7248839 Abdominal distension
72488399 7248839 Abdominal pain upper
72488399 7248839 Blood glucose increased
72488399 7248839 Blood potassium decreased
72488399 7248839 Blood pressure increased
72488399 7248839 Bone disorder
72488399 7248839 Burning sensation
72488399 7248839 Chromaturia
72488399 7248839 Decreased appetite
72488399 7248839 Diabetes mellitus
72488399 7248839 Diabetic neuropathy
72488399 7248839 Dyspnoea
72488399 7248839 Ear discomfort
72488399 7248839 Erythema
72488399 7248839 Feeling abnormal
72488399 7248839 Flushing
72488399 7248839 Headache
72488399 7248839 Hyperhidrosis
72488399 7248839 Hypoaesthesia
72488399 7248839 Injection site pain
72488399 7248839 Malignant neoplasm progression
72488399 7248839 Nausea
72488399 7248839 Neoplasm progression
72488399 7248839 Nervousness
72488399 7248839 Oedema peripheral
72488399 7248839 Pain
72488399 7248839 Pain in extremity
72488399 7248839 Paraesthesia
72488399 7248839 Peripheral swelling
72488399 7248839 Pruritus
72488399 7248839 Rash pruritic
72488399 7248839 Shock
72488399 7248839 Sinusitis
72488399 7248839 Skin discolouration
72488399 7248839 Swelling
72488399 7248839 Therapeutic response decreased
72488399 7248839 Tinnitus
72488399 7248839 Urinary tract infection
72488399 7248839 Urine abnormality

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
72488399 7248839 1 20091211 20110303 0
72488399 7248839 2 20110427 20120328 0
72488399 7248839 3 20120715 20130313 0
72488399 7248839 4 20130907 0