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
127656351 12765635 1 I 201211 20160908 20160921 20160921 EXP PHHY2016DE124614 NOVARTIS 0.00 A M Y 0.00000 20160921 CN DE DE

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
127656351 12765635 1 PS MYFORTIC MYCOPHENOLATE SODIUM 1 Unknown 720 MG, BID 50791 720 MG BID
127656351 12765635 2 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Unknown 2 MG, BID 0 2 MG CAPSULE BID
127656351 12765635 3 C PREDNISOLON PREDNISOLONE 1 Unknown 5 MG, UNK U 0 5 MG
127656351 12765635 4 C VALCYTE VALGANCICLOVIR HYDROCHLORIDE 1 Unknown 450 MG, QD Y 0 450 MG QD
127656351 12765635 5 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 5 MG, BID U 0 5 MG BID
127656351 12765635 6 C BISOPROLOL HEMIFUMARATE BISOPROLOL FUMARATE 1 Unknown UNK Y 0
127656351 12765635 7 C BISOPROLOL HEMIFUMARATE BISOPROLOL FUMARATE 1 Unknown 5 MG, QD Y 0 5 MG QD
127656351 12765635 8 C MOXONIDINE MOXONIDINE 1 Unknown 0.2 MG, UNK Y 0 .2 MG
127656351 12765635 9 C VIGANTOLETTEN CHOLECALCIFEROL 1 0
127656351 12765635 10 C DIAZEPAM. DIAZEPAM 1 Unknown 2 MG, BID U 0 2 MG TABLET BID
127656351 12765635 11 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Unknown 20 MG, QD U 0 20 MG TABLET QD
127656351 12765635 12 C MAGNESIUM VERLA TABLET 2 Unknown UNK UNK, BID U 0 BID
127656351 12765635 13 C VIGANTOLETTEN CHOLECALCIFEROL 1 1000 UNK, QD U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127656351 12765635 1 Renal transplant
127656351 12765635 2 Product used for unknown indication
127656351 12765635 3 Product used for unknown indication
127656351 12765635 4 Product used for unknown indication
127656351 12765635 5 Product used for unknown indication
127656351 12765635 6 Product used for unknown indication
127656351 12765635 8 Product used for unknown indication
127656351 12765635 10 Product used for unknown indication
127656351 12765635 11 Product used for unknown indication
127656351 12765635 12 Product used for unknown indication
127656351 12765635 13 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127656351 12765635 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127656351 12765635 Ataxia
127656351 12765635 Chronic allograft nephropathy
127656351 12765635 Chronic myeloid leukaemia
127656351 12765635 Clostridium difficile infection
127656351 12765635 Dialysis related complication
127656351 12765635 Dyskinesia
127656351 12765635 Dystonia
127656351 12765635 End stage renal disease
127656351 12765635 Eosinophilic pneumonia acute
127656351 12765635 Epiphysiolysis
127656351 12765635 Hyperparathyroidism
127656351 12765635 Hypertension
127656351 12765635 Infection in an immunocompromised host
127656351 12765635 Kidney transplant rejection
127656351 12765635 Nephrogenic anaemia
127656351 12765635 Pneumonia
127656351 12765635 Psychomotor retardation
127656351 12765635 Renal hypoplasia
127656351 12765635 Therapeutic response unexpected
127656351 12765635 Thrombocytopenia
127656351 12765635 Vein disorder

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found