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
126141711 12614171 1 I 20160729 0 20160801 20160801 DIR 48.00 YR M N 185.00000 LBS 20160729 N 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
126141711 12614171 1 PS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 0
126141711 12614171 2 C TRAMADOL. TRAMADOL 1 0
126141711 12614171 4 C ACETAMINOPHEN. ACETAMINOPHEN 1 0
126141711 12614171 6 C CARBAMAZEPINE. CARBAMAZEPINE 1 0
126141711 12614171 8 C TIZANIDINE. TIZANIDINE 1 0
126141711 12614171 9 SS SIMVASTATIN. SIMVASTATIN 1 0
126141711 12614171 11 C RISPERAQDONE 2 0
126141711 12614171 13 C NORTRIPTYLINE NORTRIPTYLINE 1 0
126141711 12614171 15 C DULOXETINE. DULOXETINE 1 0
126141711 12614171 17 C CHAMOMILE TEA MATRICARIA RECUTITA 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126141711 12614171 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126141711 12614171 Abdominal discomfort
126141711 12614171 Abdominal distension
126141711 12614171 Haematemesis
126141711 12614171 Headache
126141711 12614171 Nausea
126141711 12614171 Neck pain
126141711 12614171 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found