The Safety Rates Drug Report

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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
96938238 9693823 8 F 201307 20160808 20131118 20160812 EXP PHHY2013MX061975 NOVARTIS 81.07 YR F Y 0.00000 20160812 OT MX MX

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
96938238 9693823 1 PS DIOVAN VALSARTAN 1 Oral 1 DF, QD (320 MG) Y Z0060 21283 1 DF TABLET QD
96938238 9693823 2 SS DIOVAN VALSARTAN 1 Oral 0.5 DF (320 MG), BID (0.5 TABLET IN THE MORNING AND 0.5 TABLET AT NIGHT) Y 21283 .5 DF TABLET BID
96938238 9693823 3 SS DIOVAN VALSARTAN 1 Oral 0.5 DF, QD (320 MG, HALF TABLET) Y 20069 21283 .5 DF TABLET QD
96938238 9693823 4 SS DIOVAN VALSARTAN 1 Unknown 1 DF, QD (160 MG) Y 21283 1 DF TABLET QD
96938238 9693823 5 SS DIOVAN VALSARTAN 1 Unknown 0.5 DF (320 MG) (8 MONTHS AGO APPROX) Y 21283 .5 DF TABLET
96938238 9693823 6 C ADALAT NIFEDIPINE 1 Unknown 1 DF, QD Y 0 1 DF CAPSULE QD
96938238 9693823 7 C ADALAT NIFEDIPINE 1 Unknown 0.5 DF, QD (EVERY NIGHT) Y 0 .5 DF CAPSULE QD
96938238 9693823 8 C CRESTOR ROSUVASTATIN CALCIUM 1 Unknown 1 DF, QD 0 1 DF QD
96938238 9693823 9 C LASIX FUROSEMIDE 1 Unknown 0.5 DF, QD 0 .5 DF QD
96938238 9693823 10 C NOVOTIRAL LEVOTHYROXINE 1 Unknown 0.5 DF, QD 0 .5 DF QD
96938238 9693823 11 C RIVOTRIL CLONAZEPAM 1 Unknown 1 DF, QD 0 1 DF QD
96938238 9693823 12 C ROSUVASTATIN. ROSUVASTATIN 1 Unknown U 0
96938238 9693823 13 C ADALAT CC NIFEDIPINE 1 Unknown U 0
96938238 9693823 14 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown U 0
96938238 9693823 15 C ALDACTONE A SPIRONOLACTONE 1 Unknown U 0
96938238 9693823 16 C COLECALCIFEROL CHOLECALCIFEROL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
96938238 9693823 1 Hypertension
96938238 9693823 2 Blood pressure increased
96938238 9693823 6 Hypertension
96938238 9693823 8 Blood cholesterol abnormal
96938238 9693823 9 Diuretic therapy
96938238 9693823 10 Hypothyroidism
96938238 9693823 11 Insomnia
96938238 9693823 12 Blood cholesterol abnormal
96938238 9693823 13 Product used for unknown indication
96938238 9693823 14 Product used for unknown indication
96938238 9693823 15 Product used for unknown indication
96938238 9693823 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
96938238 9693823 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
96938238 9693823 Blood pressure decreased
96938238 9693823 Catarrh
96938238 9693823 Fall
96938238 9693823 Femur fracture
96938238 9693823 Hip fracture
96938238 9693823 Influenza
96938238 9693823 Oedema peripheral
96938238 9693823 Oropharyngeal pain
96938238 9693823 Wrong technique in product usage process

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
96938238 9693823 1 2012 0
96938238 9693823 3 201605 0
96938238 9693823 6 2012 0
96938238 9693823 8 2009 0
96938238 9693823 9 2011 0
96938238 9693823 11 2004 0