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
125076072 12507607 2 F 20160609 20160906 20160629 20160915 EXP PHHO2016FR009142 NOVARTIS 60.69 YR F Y 73.00000 KG 20160915 MD FR FR

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
125076072 12507607 1 PS CERTICAN EVEROLIMUS 1 Oral 3 MG, QD 21560 3 MG QD
125076072 12507607 2 SS PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Unknown 3 MG, QD 0 3 MG QD
125076072 12507607 3 SS PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Unknown 6 MG, QD 0 6 MG QD
125076072 12507607 4 SS CORTANCYL PREDNISONE 1 Unknown 10 MG, QD 0 10 MG QD
125076072 12507607 5 SS CORTANCYL PREDNISONE 1 Unknown UNK 0
125076072 12507607 6 C ROVALCYTE VALGANCICLOVIR HYDROCHLORIDE 1 Unknown 450 MG, QD 0 450 MG QD
125076072 12507607 7 C TEGRETOL CARBAMAZEPINE 1 Oral 400 MG, QD 0 400 MG QD
125076072 12507607 8 C LASILIX FUROSEMIDE 1 Unknown 60 MG, QD 0 60 MG QD
125076072 12507607 9 C LASILIX FUROSEMIDE 1 80 MG, QD 0 80 MG QD
125076072 12507607 10 C PREVISCAN FLUINDIONE 1 Oral 20 MG, 3/4TH TABLET, DAILY 0 TABLET
125076072 12507607 11 C KARDEGIC ASPIRIN LYSINE 1 Unknown 75 MG, QD 0 75 MG QD
125076072 12507607 12 C ATENOLOL. ATENOLOL 1 Oral 25 MG, QD Y 0 25 MG QD
125076072 12507607 13 C BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 400 MG, QD 0 400 MG QD
125076072 12507607 14 C ARANESP DARBEPOETIN ALFA 1 Unknown 60 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125076072 12507607 1 Renal transplant
125076072 12507607 2 Renal transplant
125076072 12507607 4 Renal transplant
125076072 12507607 6 Prophylaxis
125076072 12507607 7 Neuralgia
125076072 12507607 8 Peripheral artery occlusion
125076072 12507607 9 Renal failure
125076072 12507607 10 Hypercoagulation
125076072 12507607 11 Prophylaxis
125076072 12507607 12 Hypertension
125076072 12507607 13 Prophylaxis
125076072 12507607 14 Anaemia

Outcome of event

Event ID CASEID OUTC COD
125076072 12507607 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125076072 12507607 Abdominal pain
125076072 12507607 Acute pulmonary oedema
125076072 12507607 Cardiorenal syndrome
125076072 12507607 General physical health deterioration
125076072 12507607 Sinus node dysfunction
125076072 12507607 Vomiting

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
125076072 12507607 1 20160526 0
125076072 12507607 2 20150526 0
125076072 12507607 3 20160802 0
125076072 12507607 4 20150526 0
125076072 12507607 5 20160815 0
125076072 12507607 6 20160606 0
125076072 12507607 7 20160525 0
125076072 12507607 8 20160701 0
125076072 12507607 9 20160816 0
125076072 12507607 10 20160618 0
125076072 12507607 12 20160813 0
125076072 12507607 13 20160606 0
125076072 12507607 14 20160525 0