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
125969211 12596921 1 I 20150209 20160719 20160727 20160727 EXP PHHY2016DE100410 NOVARTIS 0.00 E F Y 0.00000 20160727 MD 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
125969211 12596921 1 PS AFINITOR EVEROLIMUS 1 Unknown 10 MG, UNK 22334 10 MG TABLET
125969211 12596921 2 SS LETROZOLE. LETROZOLE 1 Unknown 2.5 MG, UNK 0 2.5 MG
125969211 12596921 3 SS ZOMETA ZOLEDRONIC ACID 1 Unknown UNK U 0
125969211 12596921 4 SS BEVACIZUMAB BEVACIZUMAB 1 Unknown UNK U 0
125969211 12596921 5 SS FASLODEX FULVESTRANT 1 Unknown UNK U 0
125969211 12596921 6 C L-THYROXINE LEVOTHYROXINE 1 Unknown UNK 0
125969211 12596921 7 C SIMVA 2 Unknown 10 OT, UNK 0
125969211 12596921 8 C ASA ASPIRIN 1 Unknown 100 OT, UNK 0
125969211 12596921 9 C METOPROLOL. METOPROLOL 1 Unknown UNK 0
125969211 12596921 10 C EXFORGE HCT AMLODIPINE BESYLATEHYDROCHLOROTHIAZIDEVALSARTAN 1 Unknown UNK 0
125969211 12596921 11 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown UNK 0
125969211 12596921 12 C VALSARTAN. VALSARTAN 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125969211 12596921 1 Product used for unknown indication
125969211 12596921 2 Product used for unknown indication
125969211 12596921 3 Product used for unknown indication
125969211 12596921 4 Product used for unknown indication
125969211 12596921 5 Product used for unknown indication
125969211 12596921 6 Hypothyroidism
125969211 12596921 7 Hypercholesterolaemia
125969211 12596921 8 Haemodilution
125969211 12596921 9 Hypertension
125969211 12596921 10 Hypertension
125969211 12596921 11 Hypertension
125969211 12596921 12 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125969211 12596921 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125969211 12596921 Alopecia
125969211 12596921 Dry eye
125969211 12596921 Polyneuropathy

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
125969211 12596921 1 201208 201402 0
125969211 12596921 2 200603 201005 0