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
127769101 12776910 1 I 20160923 20160923 20160923 EXP AU-BAUSCH-BL-2016-023505 BAUSCH AND LOMB 0.00 F Y 0.00000 20160923 OT AU AU

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
127769101 12776910 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown U 40070
127769101 12776910 2 SS DEXAMETHASONE SODIUM PHOSPHATE. DEXAMETHASONE SODIUM PHOSPHATE 1 Unknown U 40069
127769101 12776910 3 C IMMUNOGLOBULIN NOS 2 0
127769101 12776910 4 C INSULIN NOS INSULIN NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127769101 12776910 1 Product used for unknown indication
127769101 12776910 2 Product used for unknown indication
127769101 12776910 3 Product used for unknown indication
127769101 12776910 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127769101 12776910 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127769101 12776910 Cushingoid
127769101 12776910 Insomnia
127769101 12776910 Irritability

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

no results found

Therapies reported

no results found