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
126051391 12605139 1 I 2014 20160726 20160729 20160729 EXP GB-MHRA-ADR 23560724 GB-009507513-1607GBR011020 MERCK 35.00 YR M Y 77.56000 KG 20160729 CN GB GB

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
126051391 12605139 1 PS MONTELUKAST SODIUM. MONTELUKAST SODIUM 1 Oral EVENING OR NIGHT BEFORE BED Y U 20829 10 MG CAPSULE
126051391 12605139 2 C ACRIVASTINE ACRIVASTINE 1 0
126051391 12605139 3 C CANDESARTAN CANDESARTAN 1 0
126051391 12605139 4 C CODEINE PHOSPHATE CODEINE PHOSPHATE 1 0
126051391 12605139 5 C SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
126051391 12605139 6 C VENTOLIN ALBUTEROL SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126051391 12605139 1 Asthma prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126051391 12605139 OT
126051391 12605139 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126051391 12605139 Anxiety
126051391 12605139 Autophobia
126051391 12605139 Depression
126051391 12605139 Malaise
126051391 12605139 Nightmare
126051391 12605139 Sleep disorder
126051391 12605139 Suicidal ideation

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
126051391 12605139 1 2014 20160707 0