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
127166851 12716685 1 I 20160728 20160829 20160906 20160906 EXP FR-PFIZER INC-2016416359 PFIZER 32.00 YR M Y 0.00000 20160906 OT FR FR

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
127166851 12716685 1 PS EUPANTOL PANTOPRAZOLE SODIUM 1 Oral UNK Y 20987
127166851 12716685 2 SS PROPOFOL. PROPOFOL 1 Intravenous (not otherwise specified) UNK Y 77908 EMULSION FOR INJECTION
127166851 12716685 3 SS LOVENOX ENOXAPARIN SODIUM 1 Subcutaneous UNK Y 0 SOLUTION FOR INJECTION
127166851 12716685 4 SS ACUPAN NEFOPAM HYDROCHLORIDE 1 Unknown UNK Y 0
127166851 12716685 5 SS PERFALGAN ACETAMINOPHEN 1 Intravenous (not otherwise specified) UNK Y 0
127166851 12716685 6 SS SUFENTANIL SUFENTANIL 1 Intravenous (not otherwise specified) UNK Y 0
127166851 12716685 7 SS PROFENID KETOPROFEN 1 Intravenous (not otherwise specified) UNK Y 0
127166851 12716685 8 SS DOLIPRANE ACETAMINOPHEN 1 Oral UNK Y 0
127166851 12716685 9 SS AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 Intravenous (not otherwise specified) 2 G, ONE SINGLE Y 0 2 G
127166851 12716685 10 SS NIMBEX CISATRACURIUM BESYLATE 1 Intravenous (not otherwise specified) UNK Y 0
127166851 12716685 11 C ESOMEPRAZOLE ESOMEPRAZOLE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127166851 12716685 1 Gastrooesophageal reflux disease
127166851 12716685 2 Induction of anaesthesia
127166851 12716685 3 Thrombosis prophylaxis
127166851 12716685 4 Pain
127166851 12716685 5 Pain
127166851 12716685 6 Induction of anaesthesia
127166851 12716685 7 Pain
127166851 12716685 8 Pain
127166851 12716685 9 Antibiotic prophylaxis
127166851 12716685 10 Induction of anaesthesia

Outcome of event

Event ID CASEID OUTC COD
127166851 12716685 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127166851 12716685 Erythema
127166851 12716685 Purpura
127166851 12716685 Rash pustular

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
127166851 12716685 1 20160726 20160801 0
127166851 12716685 2 20160727 20160727 0
127166851 12716685 3 20160727 20160801 0
127166851 12716685 4 20160727 20160727 0
127166851 12716685 5 20160727 20160727 0
127166851 12716685 6 20160727 20160727 0
127166851 12716685 7 20160727 20160727 0
127166851 12716685 8 20160727 20160801 0
127166851 12716685 9 20160727 20160727 0
127166851 12716685 10 20160727 20160727 0