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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
108805743 10880574 3 F 201103 20160919 20150303 20160927 EXP US-ASTRAZENECA-2015SE18640 ASTRAZENECA 70.00 YR F Y 78.90000 KG 20160928 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
108805743 10880574 1 SS ATENOLOL. ATENOLOL 1 Oral Y U 0 25 MG TABLET BID
108805743 10880574 2 SS ATENOLOL. ATENOLOL 1 Oral Y U 0 25 MG TABLET BID
108805743 10880574 3 SS ATENOLOL. ATENOLOL 1 Oral Y U 0 25 MG TABLET QD
108805743 10880574 4 SS ATENOLOL. ATENOLOL 1 Oral Y U 0 25 MG TABLET QD
108805743 10880574 5 SS ATENOLOL. ATENOLOL 1 Oral Y U 0 25 MG TABLET QD
108805743 10880574 6 SS ATENOLOL. ATENOLOL 1 Oral Y U 0 25 MG TABLET QD
108805743 10880574 7 SS ATENOLOL. ATENOLOL 1 Oral Y U 0 25 MG TABLET BID
108805743 10880574 8 SS ATENOLOL. ATENOLOL 1 Oral Y U 0 25 MG TABLET BID
108805743 10880574 9 PS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 21153 40 MG QD
108805743 10880574 10 SS NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 21153 40 MG QD
108805743 10880574 11 SS METOPROLOL - UNKNOWN METOPROLOL 1 Oral UNKNOWN Y 0
108805743 10880574 12 SS METOPROLOL - UNKNOWN METOPROLOL 1 Oral UNKNOWN Y 0
108805743 10880574 13 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 120 MG QD
108805743 10880574 14 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 120 MG QD
108805743 10880574 15 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 180 MG QD
108805743 10880574 16 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 180 MG QD
108805743 10880574 17 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 120 MG QD
108805743 10880574 18 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 120 MG QD
108805743 10880574 19 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 180 MG QD
108805743 10880574 20 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 180 MG QD
108805743 10880574 21 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 120 MG QD
108805743 10880574 22 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 120 MG QD
108805743 10880574 23 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 120 MG QD
108805743 10880574 24 SS CARDIZEM LA DILTIAZEM HYDROCHLORIDE 1 Oral U U 0 120 MG QD
108805743 10880574 25 C BENICAR OLMESARTAN MEDOXOMIL 1 Oral 0 40 MG QD
108805743 10880574 26 C XANAX ALPRAZOLAM 1 Oral 0 .5 MG QD
108805743 10880574 27 C BENICAR HCT HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL 1 Oral 0 40 MG QD
108805743 10880574 28 C LAXATIVE UNSPECIFIED INGREDIENT 1 Unknown UNKNOWN 0
108805743 10880574 29 C MIRALAX POLYETHYLENE GLYCOL 3350 1 Oral UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108805743 10880574 1 Heart rate increased
108805743 10880574 2 Chest pain
108805743 10880574 3 Heart rate increased
108805743 10880574 4 Chest pain
108805743 10880574 5 Heart rate increased
108805743 10880574 6 Chest pain
108805743 10880574 7 Heart rate increased
108805743 10880574 8 Chest pain
108805743 10880574 9 Gastrooesophageal reflux disease
108805743 10880574 10 Gastrooesophageal reflux disease
108805743 10880574 13 Heart rate increased
108805743 10880574 14 Chest pain
108805743 10880574 15 Heart rate increased
108805743 10880574 16 Chest pain
108805743 10880574 17 Heart rate increased
108805743 10880574 18 Chest pain
108805743 10880574 19 Heart rate increased
108805743 10880574 20 Chest pain
108805743 10880574 21 Heart rate increased
108805743 10880574 22 Chest pain
108805743 10880574 23 Heart rate increased
108805743 10880574 24 Chest pain
108805743 10880574 25 Hypertension
108805743 10880574 26 Sleep disorder
108805743 10880574 27 Hypertension
108805743 10880574 28 Bowel movement irregularity
108805743 10880574 29 Bowel movement irregularity

Outcome of event

Event ID CASEID OUTC COD
108805743 10880574 OT
108805743 10880574 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
108805743 10880574 Abdominal discomfort
108805743 10880574 Abdominal pain upper
108805743 10880574 Back disorder
108805743 10880574 Bladder discomfort
108805743 10880574 Body height decreased
108805743 10880574 Bowel movement irregularity
108805743 10880574 Cardiac disorder
108805743 10880574 Chest discomfort
108805743 10880574 Chest pain
108805743 10880574 Drug dose omission
108805743 10880574 Feeling abnormal
108805743 10880574 Gastrooesophageal reflux disease
108805743 10880574 Heart rate increased
108805743 10880574 Hypertension
108805743 10880574 Hypoacusis
108805743 10880574 Insomnia
108805743 10880574 Intentional product misuse
108805743 10880574 Irritable bowel syndrome
108805743 10880574 Muscle spasms
108805743 10880574 Musculoskeletal discomfort
108805743 10880574 Osteoarthritis
108805743 10880574 Palpitations
108805743 10880574 Panic attack
108805743 10880574 Pollakiuria
108805743 10880574 Polyp

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
108805743 10880574 9 2001 0
108805743 10880574 10 2001 0
108805743 10880574 11 201103 201103 0
108805743 10880574 12 201103 201103 0
108805743 10880574 13 201410 0
108805743 10880574 14 201410 0
108805743 10880574 19 201410 0
108805743 10880574 20 201410 0
108805743 10880574 21 201410 0
108805743 10880574 22 201410 0
108805743 10880574 25 201410 0
108805743 10880574 27 201103 201410 0

Execution Time: 0.0063509941101074 seconds (ucode:5215221). Developed by: James D. Barger

 


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