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
105432407 10543240 7 F 2012 20160816 20141027 20160822 EXP PHHY2014AR139113 NOVARTIS 85.28 YR F Y 0.00000 20160822 CN COUNTRY NOT SPECIFIED AR

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
105432407 10543240 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Unknown 20 MG, QMO 21008 20 MG /month
105432407 10543240 2 C AXUAL 2 Unknown 75 OT, QD U 0 QD
105432407 10543240 3 C KABIAN 2 Unknown 75 OT, QD U 0 QD
105432407 10543240 4 C URZAC//URSODEOXYCHOLIC ACID 2 Unknown 300 OT, BID U 0 BID
105432407 10543240 5 C ISOPHANE INSULIN INSULIN NOS 1 Unknown 26 IU (8 AND 18 IU), QD U 0 26 IU QD
105432407 10543240 6 C BIATRIX 2 Unknown 25 MG, QD U 0 25 MG QD
105432407 10543240 7 C ENDOCLAR 2 Unknown 10 MG, QD U 0 10 MG QD
105432407 10543240 8 C ULCOZOL 2 Unknown 20 MG, QD U 0 20 MG QD
105432407 10543240 9 C LOTRIAL ENALAPRIL MALEATE 1 Unknown 10 MG, BID U 0 10 MG BID
105432407 10543240 10 C LIPOCAMBI 2 Unknown 40 MG, QD U 0 40 MG QD
105432407 10543240 11 C CORBIS 2 Unknown 10 MG, QD U 0 10 MG QD
105432407 10543240 12 C CONEXINE//MEMANTINE HYDROCHLORIDE 2 Unknown 20 MG, QD U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105432407 10543240 1 Acromegaly
105432407 10543240 2 Product used for unknown indication
105432407 10543240 3 Product used for unknown indication
105432407 10543240 4 Product used for unknown indication
105432407 10543240 5 Product used for unknown indication
105432407 10543240 6 Product used for unknown indication
105432407 10543240 7 Product used for unknown indication
105432407 10543240 8 Product used for unknown indication
105432407 10543240 9 Product used for unknown indication
105432407 10543240 10 Product used for unknown indication
105432407 10543240 11 Product used for unknown indication
105432407 10543240 12 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
105432407 10543240 HO
105432407 10543240 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105432407 10543240 Abdominal discomfort
105432407 10543240 Abdominal infection
105432407 10543240 Brain neoplasm
105432407 10543240 Cardiac failure
105432407 10543240 Cardiac infection
105432407 10543240 Cerebral haemangioma
105432407 10543240 Cerebrovascular accident
105432407 10543240 Cognitive disorder
105432407 10543240 Contusion
105432407 10543240 Dementia Alzheimer's type
105432407 10543240 Discomfort
105432407 10543240 Fall
105432407 10543240 Hypotonia
105432407 10543240 Liver disorder
105432407 10543240 Memory impairment
105432407 10543240 Nail disorder
105432407 10543240 Nosocomial infection
105432407 10543240 Onychomycosis
105432407 10543240 Pain
105432407 10543240 Pneumonia
105432407 10543240 Suicidal ideation
105432407 10543240 Tachycardia
105432407 10543240 Traumatic intracranial haemorrhage
105432407 10543240 Urinary tract infection
105432407 10543240 Vein disorder

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
105432407 10543240 1 2005 0