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
127041701 12704170 1 I 20160829 20160831 20160831 PER US-ASTRAZENECA-2016SE92831 ASTRAZENECA 0.00 M Y 14.50000 KG 20160831 US 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
127041701 12704170 1 PS SYNAGIS PALIVIZUMAB 1 Intramuscular U 0 INJECTION
127041701 12704170 2 C TRILEPTAL OXCARBAZEPINE 1 0
127041701 12704170 3 C KEPPRA LEVETIRACETAM 1 0
127041701 12704170 4 C KLONOPIN CLONAZEPAM 1 0
127041701 12704170 5 C VALPROIC ACID. VALPROIC ACID 1 0
127041701 12704170 6 C RANITIDINE. RANITIDINE 1 0
127041701 12704170 7 C DIASTAT DIAZEPAM 1 0
127041701 12704170 8 C ERYPED ERYTHROMYCIN ETHYLSUCCINATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127041701 12704170 8 Impaired gastric emptying

Outcome of event

Event ID CASEID OUTC COD
127041701 12704170 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127041701 12704170 Respiratory syncytial virus infection
127041701 12704170 Sputum retention

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
127041701 12704170 1 201210 0