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
126565031 12656503 1 I 20160809 20160816 20160816 EXP GB-MHRA-EYC 00143337 GB-MYLANLABS-2016M1033472 MYLAN 0.00 Y 0.00000 20160816 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
126565031 12656503 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral ALTERNATING WITH 7.5MG U U 77042 5 MG
126565031 12656503 2 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral ALTERNATING WITH 5MG U U 77042 7.5 MG
126565031 12656503 3 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 10 MG, UNK U U 77042 10 MG
126565031 12656503 4 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 20 MG, UNK U U 77042 20 MG
126565031 12656503 5 C PREDNISOLONE ACTAVIS PREDNISOLONE 1 UNK U 0
126565031 12656503 6 C SULPHASALAZINE SULFASALAZINE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126565031 12656503 1 Anxiety
126565031 12656503 2 Anxiety

Outcome of event

Event ID CASEID OUTC COD
126565031 12656503 HO
126565031 12656503 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126565031 12656503 Blood pressure decreased
126565031 12656503 Heart rate abnormal
126565031 12656503 Palpitations
126565031 12656503 Syncope
126565031 12656503 Ventricular tachycardia

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
126565031 12656503 5 1997 0