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
127182081 12718208 1 I 201503 20160824 20160906 20160906 EXP SE-MPA-2016-004634 SE-SA-2016SA157327 AVENTIS 54.00 YR A F Y 0.00000 20160906 CN SE SE

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
127182081 12718208 1 PS ALLEGRA FEXOFENADINE HYDROCHLORIDE 1 Unknown Y UNKNOWN 20872
127182081 12718208 2 SS LOSARTAN. LOSARTAN 1 Unknown U UNKNOWN 0
127182081 12718208 3 SS HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown U UNKNOWN 0
127182081 12718208 4 SS METOPROLOL. METOPROLOL 1 Unknown U UNKNOWN 0
127182081 12718208 5 SS ENALAPRIL ENALAPRIL 1 Unknown U UNKNOWN 0
127182081 12718208 6 SS FELODIPINE. FELODIPINE 1 Unknown Y UNKNOWN 0
127182081 12718208 7 SS SIMVASTATIN. SIMVASTATIN 1 Unknown Y UNKNOWN 0
127182081 12718208 8 SS AMLODIPINE AMLODIPINE BESYLATE 1 Unknown Y U UNKNOWN 0
127182081 12718208 9 SS OMEPRAZOLE. OMEPRAZOLE 1 Unknown Y UNKNOWN 0
127182081 12718208 10 C VITAMIN D CHOLECALCIFEROL 1 Unknown 0
127182081 12718208 11 C SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127182081 12718208 1 Hypersensitivity
127182081 12718208 2 Hypertension
127182081 12718208 4 Hypertension
127182081 12718208 5 Hypertension
127182081 12718208 6 Hypertension
127182081 12718208 7 Lipids increased
127182081 12718208 8 Hypertension
127182081 12718208 9 Chest pain

Outcome of event

Event ID CASEID OUTC COD
127182081 12718208 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127182081 12718208 Arthralgia
127182081 12718208 Back pain
127182081 12718208 Chest discomfort
127182081 12718208 Chest pain
127182081 12718208 Dry eye
127182081 12718208 Fatigue
127182081 12718208 Oropharyngeal pain
127182081 12718208 Peripheral swelling
127182081 12718208 Pharyngeal oedema
127182081 12718208 Sleep disorder

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
127182081 12718208 1 2012 201505 0
127182081 12718208 3 201302 0
127182081 12718208 6 201304 201606 0
127182081 12718208 7 201503 201503 0
127182081 12718208 8 2013 2013 0
127182081 12718208 9 2013 2015 0
127182081 12718208 10 201301 0
127182081 12718208 11 2013 0