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
125482861 12548286 1 I 20160708 20160712 20160712 EXP CA-BAUSCH-BL-2016-016481 BAUSCH AND LOMB 0.00 F Y 0.00000 20160712 OT CA CA

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
125482861 12548286 1 PS CLINDAMYCIN CLINDAMYCINCLINDAMYCIN PHOSPHATE 1 Unknown U 50782
125482861 12548286 2 SS CLINDAMYCIN CLINDAMYCINCLINDAMYCIN PHOSPHATE 1 U 50782
125482861 12548286 3 SS PANTOLOC PANTOPRAZOLE SODIUM 1 Unknown U 0 ENTERIC-COATED TABLET
125482861 12548286 4 SS PANTOLOC PANTOPRAZOLE SODIUM 1 U 0
125482861 12548286 5 C PROBACLAC 2 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125482861 12548286 1 Oropharyngeal pain
125482861 12548286 2 Cough
125482861 12548286 3 Oropharyngeal pain
125482861 12548286 4 Pain
125482861 12548286 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125482861 12548286 HO
125482861 12548286 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125482861 12548286 Clostridium difficile infection
125482861 12548286 Malaise
125482861 12548286 Vitamin B12 decreased
125482861 12548286 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found