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
121818333 12181833 3 F 201603 20160809 20160315 20160817 EXP US-ASTRAZENECA-2016SE25446 ASTRAZENECA 824.00 MON F Y 131.50000 KG 20160817 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
121818333 12181833 1 PS MOVANTIK NALOXEGOL OXALATE 1 Oral 204760 25 MG TABLET QD
121818333 12181833 2 SS MOVANTIK NALOXEGOL OXALATE 1 Oral 204760 25 MG TABLET QD
121818333 12181833 3 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral 0 40 MG QD
121818333 12181833 4 C SAVELLA MILNACIPRAN HYDROCHLORIDE 1 Oral 0 150 MG BID
121818333 12181833 5 C ONDANSETRON ONDANSETRON 1 Oral 4.0MG AS REQUIRED 0 4 MG
121818333 12181833 6 C METHENAMINE HIPP TAB 2 Oral 0 1 G TABLET BID
121818333 12181833 7 C CELCOXIB 2 Oral 0 200 MG QD
121818333 12181833 8 C VITAMIN D CHOLECALCIFEROL 1 Oral 0 BIW
121818333 12181833 9 C FUROSEMIDE. FUROSEMIDE 1 Oral 0 80 MG BID
121818333 12181833 10 C METOLACONE 2 Oral 0 5 MG BID
121818333 12181833 11 C AMITIZA LUBIPROSTONE 1 Oral TWO TIMES A DAY 0
121818333 12181833 12 C LINZESS LINACLOTIDE 1 Oral 0 290 UG QD
121818333 12181833 13 C FETCIMA 2 Oral 0 80 MG QD
121818333 12181833 14 C XANAX ALPRAZOLAM 1 Oral 2.0MG AS REQUIRED 0 2 MG
121818333 12181833 15 C GABAPENTIN. GABAPENTIN 1 Oral 800.0MG AS REQUIRED 0 800 MG
121818333 12181833 16 C SIMVASTATIN. SIMVASTATIN 1 Oral 0 40 MG QD
121818333 12181833 17 C 3 VITAMIN COMPOUND 2 Oral 1 DAILY 0
121818333 12181833 18 C CENTRUM SILVER VITAMIN 2 Oral 1 DAILY 0
121818333 12181833 19 C HYDROCODONE HYDROCODONE 1 10/325MG 1 EVERY SIX HOURS AS NEEDED FOR PAIN IN KNEES FROM FALLS 0
121818333 12181833 20 C SODIUM BICARBONATE. SODIUM BICARBONATE 1 TWO TIMES A DAY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121818333 12181833 1 Bowel movement irregularity
121818333 12181833 2 Constipation
121818333 12181833 3 Hiatus hernia
121818333 12181833 4 Blood pressure abnormal
121818333 12181833 5 Nausea
121818333 12181833 6 Infection
121818333 12181833 7 Rheumatoid arthritis
121818333 12181833 8 Vitamin D decreased
121818333 12181833 9 Oedema peripheral
121818333 12181833 10 Fibromyalgia
121818333 12181833 11 Gastrointestinal disorder
121818333 12181833 12 Abdominal discomfort
121818333 12181833 13 Ill-defined disorder
121818333 12181833 14 Panic attack
121818333 12181833 15 Fibromyalgia
121818333 12181833 16 Blood cholesterol abnormal
121818333 12181833 17 Hypovitaminosis
121818333 12181833 18 Asthenia
121818333 12181833 20 Hiatus hernia

Outcome of event

Event ID CASEID OUTC COD
121818333 12181833 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121818333 12181833 Arthralgia
121818333 12181833 Confusional state
121818333 12181833 Fall
121818333 12181833 Fear of falling
121818333 12181833 Gait disturbance
121818333 12181833 Hiatus hernia
121818333 12181833 Incontinence
121818333 12181833 Inflammation
121818333 12181833 Infrequent bowel movements
121818333 12181833 Nausea
121818333 12181833 Neoplasm malignant
121818333 12181833 Product use issue
121818333 12181833 Stress

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
121818333 12181833 1 201510 0
121818333 12181833 2 201510 0
121818333 12181833 18 201603 0