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
123566072 12356607 2 F 2014 20160510 20160511 20160813 PER US-ASTRAZENECA-2016SE34392 ASTRAZENECA 72.00 YR F Y 53.50000 KG 20160813 US US

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
123566072 12356607 1 SS ATENOLOL. ATENOLOL 1 Oral 164400 MG 0 50 MG TABLET QD
123566072 12356607 2 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 80-4.5 TWO PUFFS, TWO TIMES A DAY. 2000341F00 21929 BID
123566072 12356607 3 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral 7320 MG 0 20 MG QD
123566072 12356607 4 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral CUTS 10MG IN HALF AND TAKES A HALF ON ONE DAY AND THE SECOND HALF THE NEXT DAY. 0 TABLET
123566072 12356607 5 C PROPAIR 2 Respiratory (inhalation) AS REQUIRED 0
123566072 12356607 6 C LOSARTAN. LOSARTAN 1 Oral 0 100 MG QD
123566072 12356607 7 C MONTELUCAST SOD 2 Rectal 0 10 MG QD
123566072 12356607 8 C LEVOTHYROXINE. LEVOTHYROXINE 1 Oral 0 50 UG QD
123566072 12356607 9 C ZOLPIDEM TARTRATE. ZOLPIDEM TARTRATE 1 Oral 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123566072 12356607 1 Blood pressure abnormal
123566072 12356607 2 Asthma
123566072 12356607 3 Gastrooesophageal reflux disease
123566072 12356607 4 Blood cholesterol
123566072 12356607 5 Inhalation therapy
123566072 12356607 6 Blood pressure abnormal
123566072 12356607 7 Asthma
123566072 12356607 8 Hypothyroidism
123566072 12356607 9 Insomnia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123566072 12356607 Asthma
123566072 12356607 Blood cholesterol increased
123566072 12356607 Blood pressure increased
123566072 12356607 Intentional device misuse
123566072 12356607 Intentional product misuse
123566072 12356607 Product quality issue
123566072 12356607 Underdose

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
123566072 12356607 1 2006 0
123566072 12356607 2 2014 0
123566072 12356607 3 2014 0
123566072 12356607 4 2015 0
123566072 12356607 6 2015 0
123566072 12356607 7 2013 0
123566072 12356607 8 1996 0
123566072 12356607 9 2008 0