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
105254418 10525441 8 F 201303 20160830 20141017 20160907 EXP PHHY2014BR132561 SANDOZ 74.07 YR F Y 71.00000 KG 20160907 MD BR BR

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
105254418 10525441 1 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, EVERY 28 DAYS U 0 30 MG VIAL /month
105254418 10525441 2 SS GALVUS VILDAGLIPTIN 1 Unknown 2 DF, QD 0 2 DF TABLET QD
105254418 10525441 3 SS GALVUS VILDAGLIPTIN 1 Unknown 3 DF, QD 0 3 DF TABLET QD
105254418 10525441 4 PS METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown 3 DF, QD 75985 3 DF QD
105254418 10525441 5 SS CABERGOLINA CABERGOLINE 1 Unknown 1 DF, QW 0 1 DF TABLET /wk
105254418 10525441 6 SS CABERGOLINA CABERGOLINE 1 Unknown 2 DF, QW X170A 0 2 DF TABLET /wk
105254418 10525441 7 SS CABERGOLINA CABERGOLINE 1 Unknown 6 DF, QW 0 6 DF TABLET /wk
105254418 10525441 8 SS GLIMEPIRIDA GLIMEPIRIDE 1 Unknown 6 MG, QD Y 0 6 MG TABLET QD
105254418 10525441 9 C AVASTIN BEVACIZUMAB 1 Unknown 1 DF, UNK Y 0 1 DF
105254418 10525441 10 C ATENOLOL. ATENOLOL 1 Unknown 50 MG, QD 0 50 MG TABLET QD
105254418 10525441 11 C ATENOLOL. ATENOLOL 1 Unknown 100 MG, QD 0 100 MG TABLET QD
105254418 10525441 12 C MODURETIC 5-50 AMILORIDE HYDROCHLORIDEHYDROCHLOROTHIAZIDE 1 Unknown 1 DF, QD 0 1 DF TABLET QD
105254418 10525441 13 C MODURETIC 5-50 AMILORIDE HYDROCHLORIDEHYDROCHLOROTHIAZIDE 1 0 TABLET
105254418 10525441 14 C AMLODIPINA//AMLODIPINE 2 Unknown 1 DF, Q12H 0 1 DF TABLET Q12H
105254418 10525441 15 C PURAN LEVOTHYROXINE SODIUM 1 Unknown 1 DF, FASTING PER DAY 0 1 DF TABLET
105254418 10525441 16 C ALPRAZOLAM. ALPRAZOLAM 1 Unknown 1 DF, AT BEDTIME 0 1 DF TABLET
105254418 10525441 17 C ALPRAZOLAM. ALPRAZOLAM 1 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105254418 10525441 1 Acromegaly
105254418 10525441 2 Diabetes mellitus
105254418 10525441 4 Product used for unknown indication
105254418 10525441 5 Acromegaly
105254418 10525441 8 Diabetes mellitus
105254418 10525441 9 Visual impairment
105254418 10525441 10 Hypertension
105254418 10525441 12 Hypertension
105254418 10525441 13 Diuretic therapy
105254418 10525441 14 Hypertension
105254418 10525441 15 Hormone replacement therapy
105254418 10525441 16 Insomnia
105254418 10525441 17 Stress

Outcome of event

Event ID CASEID OUTC COD
105254418 10525441 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105254418 10525441 Blood pressure decreased
105254418 10525441 Body height decreased
105254418 10525441 Bone disorder
105254418 10525441 Decreased appetite
105254418 10525441 Diabetes mellitus
105254418 10525441 Dysuria
105254418 10525441 Feeling hot
105254418 10525441 Gait disturbance
105254418 10525441 Headache
105254418 10525441 Hypokinesia
105254418 10525441 Injection site erythema
105254418 10525441 Injection site nodule
105254418 10525441 Injection site pain
105254418 10525441 Limb discomfort
105254418 10525441 Malaise
105254418 10525441 Mass
105254418 10525441 Nodule
105254418 10525441 Pain
105254418 10525441 Pain in extremity
105254418 10525441 Thyroid disorder
105254418 10525441 Venous occlusion
105254418 10525441 Vision blurred
105254418 10525441 Vitamin D decreased
105254418 10525441 Weight decreased
105254418 10525441 Weight increased

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
105254418 10525441 1 2010 0
105254418 10525441 2 201304 0
105254418 10525441 8 2013 0
105254418 10525441 9 20140216 20140216 0