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
125090253 12509025 3 F 20151130 20160824 20160629 20160831 EXP GB-ACTAVISPR-2016-12100 GB-FRI-1000085602 FOREST 50.57 YR F Y 0.00000 20160831 OT DK 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
125090253 12509025 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 10 MG ONCE DAILY 20822 10 MG QD
125090253 12509025 2 SS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 20 MG ONCE DAILY 20822 20 MG QD
125090253 12509025 3 C LANSOPRAZOLE. LANSOPRAZOLE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125090253 12509025 1 Anxiety
125090253 12509025 3 Abdominal pain

Outcome of event

Event ID CASEID OUTC COD
125090253 12509025 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125090253 12509025 Abdominal pain upper
125090253 12509025 Cerebral haemorrhage
125090253 12509025 Cerebrovascular accident
125090253 12509025 Head injury

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
125090253 12509025 1 2008 0