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
127730041 12773004 1 I 20160804 20160922 20160922 PER US-ALLERGAN-1665026US ALLERGAN 0.00 M Y 114.29000 KG 20160922 OT 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
127730041 12773004 1 PS DAPSONE UNK DAPSONE 1 Oral 50 MG, BID U 21794 50 MG BID
127730041 12773004 2 C REVLIMID LENALIDOMIDE 1 Oral 25 MG, QD U 0 25 MG QD
127730041 12773004 3 C ACYCLOVIR. ACYCLOVIR 1 Oral 400 MG, BID U 0 400 MG BID
127730041 12773004 4 C DECADRON DEXAMETHASONE 1 Oral 4 MG, QD U 0 4 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127730041 12773004 1 Prophylaxis
127730041 12773004 2 Plasma cell myeloma
127730041 12773004 3 Prophylaxis
127730041 12773004 4 Plasma cell myeloma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127730041 12773004 Dizziness
127730041 12773004 Dyspnoea exertional
127730041 12773004 Flatulence
127730041 12773004 Lethargy
127730041 12773004 Oropharyngeal pain

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
127730041 12773004 1 20160628 0
127730041 12773004 2 20160628 0
127730041 12773004 3 20160628 0