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
126261721 12626172 1 I 201604 20160727 20160805 20160805 EXP US-TEVA-681037USA TEVA 66.74 YR F Y 47.22000 KG 20160805 OT 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
126261721 12626172 1 PS HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown Y 83177
126261721 12626172 2 SS FAMOTIDINE. FAMOTIDINE 1 Unknown U 75311
126261721 12626172 3 SS TYVASO TREPROSTINIL 1 Respiratory (inhalation) 2.4 MILLIGRAM/MILLILITERS DAILY; 18-54 MCG, (3 TO 9 BREATHS) U 2100760 0 INHALATION GAS QID
126261721 12626172 4 C TRACLEER BOSENTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126261721 12626172 1 Product used for unknown indication
126261721 12626172 2 Product used for unknown indication
126261721 12626172 3 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
126261721 12626172 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126261721 12626172 Headache
126261721 12626172 Nasopharyngitis
126261721 12626172 Nausea
126261721 12626172 Oedema
126261721 12626172 Pain in extremity
126261721 12626172 Palpitations
126261721 12626172 Pyrexia
126261721 12626172 Tachycardia
126261721 12626172 Vomiting
126261721 12626172 Wrong drug administered

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
126261721 12626172 3 20111121 0