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
106710124 10671012 4 F 20141211 20160711 20141223 20160715 EXP CN-ASTELLAS-2014US020778 ASTELLAS 45.08 YR M Y 0.00000 20160715 CN CN CN

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
106710124 10671012 1 PS TACROLIMUS. TACROLIMUS 1 Oral 2096 MG Y 204096 8 MG MODIFIED-RELEASE CAPSULE, HARD QD
106710124 10671012 2 SS TACROLIMUS. TACROLIMUS 1 Unknown UNK, UNKNOWN FREQ. 2096 MG 1M4247D 204096 MODIFIED-RELEASE CAPSULE, HARD
106710124 10671012 3 SS TACROLIMUS. TACROLIMUS 1 Unknown UNK UNK, UNKNOWN FREQ. 2096 MG 1M4266F 204096 MODIFIED-RELEASE CAPSULE, HARD
106710124 10671012 4 SS TACROLIMUS. TACROLIMUS 1 Unknown UNK, UNKNOWN FREQ. 2096 MG 1M4247D 204096 MODIFIED-RELEASE CAPSULE, HARD
106710124 10671012 5 SS TACROLIMUS. TACROLIMUS 1 Unknown UNK, UNKNOWN FREQ. 2096 MG 1M4281B 204096 MODIFIED-RELEASE CAPSULE, HARD
106710124 10671012 6 SS TACROLIMUS. TACROLIMUS 1 Unknown UNK UNK, UNKNOWN FREQ. 2096 MG 1M4266F 204096 MODIFIED-RELEASE CAPSULE, HARD
106710124 10671012 7 SS TACROLIMUS. TACROLIMUS 1 Oral 1.5 MG IN THE MORNING, 1 MG IN THE EVENING 2096 MG 1M4306F 204096 2.5 MG MODIFIED-RELEASE CAPSULE, HARD QD
106710124 10671012 8 SS TACROLIMUS. TACROLIMUS 1 Oral 2096 MG OM4033G 204096 2.5 MG MODIFIED-RELEASE CAPSULE, HARD QD
106710124 10671012 9 SS ATG-FRESENIUS LAPINE T-LYMPHOCYTE IMMUNE GLOBULIN 1 Intravenous (not otherwise specified) 550 MG, ONCE 0 550 MG INJECTION
106710124 10671012 10 C MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Oral 208500 MG U 0 750 MG TABLET QD
106710124 10671012 11 C MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Oral 208500 MG U 0 480 MG TABLET BID
106710124 10671012 12 C PREDNISON PREDNISONE 1 Oral 4020 MG U 0 15 MG TABLET QD
106710124 10671012 13 C AMLODIPINE BESYLATE. AMLODIPINE BESYLATE 1 Oral 10 MG (DAILY DOSE), TWICE DAILY U 0 10 MG TABLET BID
106710124 10671012 14 C BENAZEPRIL HYDROCHLORIDE. BENAZEPRIL HYDROCHLORIDE 1 Oral 10 MG (DAILY DOSE), TWICE DAILY U 0 10 MG TABLET BID
106710124 10671012 15 C DILTIAZEM /00489702/ 2 Oral 60 MG (DAILY DOSE), TWICE DAILY U 0 60 MG FORMULATION UNKNOWN BID
106710124 10671012 16 C ACARBOSE. ACARBOSE 1 Oral 150 MG (DAILY DOSE), THRICE DAILY U 0 150 MG FORMULATION UNKNOWN TID
106710124 10671012 17 C METFORMIN METFORMIN HYDROCHLORIDE 1 Oral U 0 500 MG FORMULATION UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106710124 10671012 1 Renal transplant
106710124 10671012 9 Renal transplant
106710124 10671012 10 Renal transplant
106710124 10671012 12 Renal transplant
106710124 10671012 13 Hypertension
106710124 10671012 14 Hypertension
106710124 10671012 15 Hypertension
106710124 10671012 16 Diabetes mellitus
106710124 10671012 17 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
106710124 10671012 HO
106710124 10671012 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106710124 10671012 Diabetes mellitus

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
106710124 10671012 1 20140325 20141216 0
106710124 10671012 2 20140307 20140425 0
106710124 10671012 3 20140426 20140526 0
106710124 10671012 4 20140527 20140627 0
106710124 10671012 5 20140628 20140828 0
106710124 10671012 6 20140828 20141216 0
106710124 10671012 7 20141217 20141219 0
106710124 10671012 8 20141220 0
106710124 10671012 9 20140307 20140307 0
106710124 10671012 10 20140309 20141217 0
106710124 10671012 11 20141218 0
106710124 10671012 12 20140319 20141217 0