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
125714881 12571488 1 I 2015 20151119 20160719 20160719 PER US-BAUSCH-BL-2015-027481 BAUSCH AND LOMB 0.00 F Y 0.00000 20160719 CN 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
125714881 12571488 1 PS XIFAXAN RIFAXIMIN 1 Oral PMWN 21361 550 MG TABLET TID
125714881 12571488 2 SS XIFAXAN RIFAXIMIN 1 Oral PMWN 21361 TABLET TID
125714881 12571488 3 SS ZITHROMAX AZITHROMYCIN DIHYDRATE 1 Oral 0
125714881 12571488 4 C ATENOLOL. ATENOLOL 1 Oral 0
125714881 12571488 5 C ESTRACE ESTRADIOL 1 0
125714881 12571488 6 C FLORASTOR SACCHAROMYCES CEREVISIAE 1 Oral 0
125714881 12571488 7 C VITAMIN D CHOLECALCIFEROL 1 Oral 0
125714881 12571488 8 C VITAMIN B VITAMIN B 1 Oral 0
125714881 12571488 9 C OXYCODONE OXYCODONE 1 Oral 0
125714881 12571488 10 C XANAX ALPRAZOLAM 1 Oral AS NEEDED 0
125714881 12571488 11 C PERCODAN ASPIRINOXYCODONE HYDROCHLORIDE 1 0
125714881 12571488 12 C ESTROGEN ESTRONESUS SCROFA OVARY 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125714881 12571488 1 Irritable bowel syndrome
125714881 12571488 3 Bronchitis
125714881 12571488 4 Hypertension
125714881 12571488 5 Product used for unknown indication
125714881 12571488 6 Product used for unknown indication
125714881 12571488 7 Product used for unknown indication
125714881 12571488 8 Product used for unknown indication
125714881 12571488 9 Product used for unknown indication
125714881 12571488 10 Relaxation therapy
125714881 12571488 11 Product used for unknown indication
125714881 12571488 12 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125714881 12571488 Bronchitis
125714881 12571488 Choking
125714881 12571488 Diarrhoea
125714881 12571488 Drug dose omission
125714881 12571488 Dysphagia
125714881 12571488 Faeces discoloured
125714881 12571488 Insomnia
125714881 12571488 Pelvic floor muscle weakness

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
125714881 12571488 1 201510 0
125714881 12571488 2 20151121 0
125714881 12571488 3 201511 0