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
93727453 9372745 3 F 1999 20160718 20130627 20160726 EXP US-ASTRAZENECA-2013SE47427 ASTRAZENECA 57.00 YR M Y 83.90000 KG 20160726 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
93727453 9372745 1 PS TENORMIN ATENOLOL 1 Oral 50 DAILY IN THE AM AND 25 MG IN THE EVENING AS NEEDED 0 TABLET
93727453 9372745 2 SS BRILINTA TICAGRELOR 1 Oral 0 90 MG TABLET BID
93727453 9372745 3 SS AMOXICILLIN. AMOXICILLIN 1 Unknown 3 COURSES OF 500 MG THREE TIMES A DAY FOR 10 DAYS U U 0
93727453 9372745 4 SS AMOXICILLIN. AMOXICILLIN 1 Unknown 2000.0MG AS REQUIRED U U 0 2000 MG
93727453 9372745 5 SS BIAXIN CLARITHROMYCIN 1 Unknown 500 MG TWO TIMES A DAY FOR 5 DAYS Y U 0
93727453 9372745 6 SS ZITHROMAX AZITHROMYCIN DIHYDRATE 1 Unknown NON AZ PRODUCT U U 0
93727453 9372745 7 SS LEVAQUIN LEVOFLOXACIN 1 Unknown U U 0
93727453 9372745 8 SS OTHER ANTIBIOTICS UNSPECIFIED INGREDIENT 1 Unknown U U 0
93727453 9372745 9 C ASPIRIN. ASPIRIN 1 0 325 MG QD
93727453 9372745 10 C VIAGRA SILDENAFIL CITRATE 1 25.0MG AS REQUIRED 0 25 MG
93727453 9372745 11 C NASOCORT BUDESONIDE 1 1 -2 SPRAYS, PRN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93727453 9372745 1 Arrhythmia
93727453 9372745 2 Acute coronary syndrome
93727453 9372745 3 Antibiotic prophylaxis
93727453 9372745 4 Antibiotic prophylaxis
93727453 9372745 5 Bronchitis
93727453 9372745 6 Bronchitis
93727453 9372745 7 Bronchitis
93727453 9372745 8 Bronchitis
93727453 9372745 9 Prophylaxis
93727453 9372745 11 Multiple allergies

Outcome of event

Event ID CASEID OUTC COD
93727453 9372745 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
93727453 9372745 Abdominal discomfort
93727453 9372745 Arrhythmia
93727453 9372745 Blood pressure fluctuation
93727453 9372745 Body height decreased
93727453 9372745 Bronchitis
93727453 9372745 Dyspnoea
93727453 9372745 Escherichia infection
93727453 9372745 Flatulence
93727453 9372745 Intentional product misuse
93727453 9372745 Lower respiratory tract infection
93727453 9372745 Myocardial infarction
93727453 9372745 Pyrexia
93727453 9372745 Seasonal allergy

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
93727453 9372745 2 2016 0
93727453 9372745 5 20130225 0