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
122409412 12240941 2 F 20160216 20161104 20160406 20160406 EXP GB-DEXPHARM-20160478 DEXCEL 61.00 YR A F Y 92.52000 KG 20161108 OT 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
122409412 12240941 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral ONE TWICE DAILY FOR 3 DAYS THEN ONE DAILY 2 DF D U LC22686 0 1 DF BID
122409412 12240941 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral ONE TWICE DAILY FOR 3 DAYS THEN ONE DAILY 3 DF Y U LC22686 0 1 DF QD
122409412 12240941 3 C ATORVASTATIN ATORVASTATIN 1 0
122409412 12240941 4 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 0
122409412 12240941 5 C CYCLIZINE CYCLIZINE 1 0
122409412 12240941 6 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
122409412 12240941 7 C PARACETAMOL ACETAMINOPHEN 1 0
122409412 12240941 8 SS PAZOPANIB PAZOPANIB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122409412 12240941 1 Abdominal pain
122409412 12240941 2 Abdominal pain

Outcome of event

Event ID CASEID OUTC COD
122409412 12240941 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122409412 12240941 Arthralgia
122409412 12240941 Contusion
122409412 12240941 Dyspnoea
122409412 12240941 Joint swelling
122409412 12240941 Liver function test increased
122409412 12240941 Peripheral swelling

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
122409412 12240941 1 20160215 20160218 0
122409412 12240941 2 20160219 20160305 0