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
798340714 7983407 14 F 20140705 20160823 20110609 20160831 EXP US-ASTRAZENECA-2010SE48550 ASTRAZENECA 20819.00 DY M Y 85.30000 KG 20160831 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
798340714 7983407 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral Y U 21366 10 MG TABLET BID
798340714 7983407 2 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral Y U 21366 10 MG TABLET QD
798340714 7983407 3 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral Y U 21366 20 MG TABLET QD
798340714 7983407 4 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral Y U 21366 10 MG TABLET QD
798340714 7983407 5 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral Y U 21366 5 MG TABLET QD
798340714 7983407 6 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral Y U 21366 10 MG TABLET BID
798340714 7983407 7 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral CUTTING PILLS IN HALF Y U 21366 TABLET
798340714 7983407 8 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral Y U 21366 10 MG TABLET QD
798340714 7983407 9 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral Y U 21366 5 MG TABLET QD
798340714 7983407 10 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral Y U 21366 TABLET
798340714 7983407 11 C PLAVIX CLOPIDOGREL BISULFATE 1 0
798340714 7983407 12 C AVAPRO IRBESARTAN 1 Oral 0 35 MG BID
798340714 7983407 13 C AVAPRO IRBESARTAN 1 Oral 35 MG UP TO 3 TIMES A DAY IF BLOOD PRESSURE IS UNDER 120 0
798340714 7983407 14 C ZETIA EZETIMIBE 1 0
798340714 7983407 15 C VALIUM DIAZEPAM 1 EITHER 2.5 MG OR 5 MG, AS NEEDED 0
798340714 7983407 16 C AVALIDE HYDROCHLOROTHIAZIDEIRBESARTAN 1 300/12.5 MG EVERY DAY 0
798340714 7983407 17 C BYSTOLIC NEBIVOLOL HYDROCHLORIDE 1 0 5 MG BID
798340714 7983407 18 C BYSTOLIC NEBIVOLOL HYDROCHLORIDE 1 0 2.5 MG BID
798340714 7983407 19 C LASIX FUROSEMIDE 1 0 20 MG QD
798340714 7983407 20 C LASIX FUROSEMIDE 1 0 20 MG QD
798340714 7983407 21 C PROTONIX PANTOPRAZOLE SODIUM 1 Oral PRN 0
798340714 7983407 22 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 10/325 , AS NEEDED/AT SOME POINT HE WAS TAKING THIS 3-4 TIMES DAILY 0
798340714 7983407 23 C TYLENOL ACETAMINOPHEN 1 10/325 AS NEEDED 0
798340714 7983407 24 C AMBIEN ZOLPIDEM TARTRATE 1 Oral 2.5MG AS REQUIRED 0 2.5 MG
798340714 7983407 25 C IRBESARTAN. IRBESARTAN 1 Oral 0 35 MG BID
798340714 7983407 26 C ASA ASPIRIN 1 0 81 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
798340714 7983407 1 Blood cholesterol abnormal
798340714 7983407 2 Blood cholesterol abnormal
798340714 7983407 3 Blood cholesterol abnormal
798340714 7983407 4 Blood cholesterol abnormal
798340714 7983407 5 Blood cholesterol abnormal
798340714 7983407 6 Blood cholesterol abnormal
798340714 7983407 7 Blood cholesterol abnormal
798340714 7983407 8 Blood cholesterol abnormal
798340714 7983407 9 Blood cholesterol abnormal
798340714 7983407 10 Blood cholesterol abnormal
798340714 7983407 12 Blood pressure abnormal
798340714 7983407 13 Blood pressure abnormal
798340714 7983407 15 Anxiety
798340714 7983407 17 Blood pressure abnormal
798340714 7983407 18 Blood pressure abnormal
798340714 7983407 19 Diuretic therapy
798340714 7983407 20 Oedema
798340714 7983407 21 Hyperchlorhydria
798340714 7983407 22 Pain
798340714 7983407 23 Pain
798340714 7983407 24 Sleep disorder
798340714 7983407 25 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
798340714 7983407 HO
798340714 7983407 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
798340714 7983407 Abasia
798340714 7983407 Abdominal discomfort
798340714 7983407 Abdominal pain
798340714 7983407 Aggression
798340714 7983407 Anxiety
798340714 7983407 Aortic rupture
798340714 7983407 Aortic stenosis
798340714 7983407 Asthma
798340714 7983407 Back pain
798340714 7983407 Blood cholesterol increased
798340714 7983407 Carotid artery stenosis
798340714 7983407 Cerebrovascular disorder
798340714 7983407 Chromaturia
798340714 7983407 Coronary artery disease
798340714 7983407 Coronary artery occlusion
798340714 7983407 Dyslexia
798340714 7983407 Dysuria
798340714 7983407 Fall
798340714 7983407 Haemorrhage
798340714 7983407 Hyperlipidaemia
798340714 7983407 Hypertension
798340714 7983407 Hypotension
798340714 7983407 Intentional product misuse
798340714 7983407 Muscle spasms
798340714 7983407 Myalgia
798340714 7983407 Myocardial infarction
798340714 7983407 Neurofibromatosis
798340714 7983407 Off label use
798340714 7983407 Panic attack
798340714 7983407 Prostatic disorder
798340714 7983407 Protein urine present
798340714 7983407 Rotator cuff syndrome
798340714 7983407 Speech disorder
798340714 7983407 Splenic rupture
798340714 7983407 Tooth fracture
798340714 7983407 Urine analysis abnormal
798340714 7983407 Visual impairment
798340714 7983407 Weight decreased

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
798340714 7983407 6 2006 0
798340714 7983407 9 2015 0
798340714 7983407 18 2015 0
798340714 7983407 24 2014 0