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
126192353 12619235 3 F 20160731 20160824 20160803 20160825 EXP US-GILEAD-2016-0226484 GILEAD 8.00 YR C M Y 0.00000 20160825 CN 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
126192353 12619235 1 PS AMBRISENTAN AMBRISENTAN 1 Oral 5 MG, QD 1412805A 22081 5 MG TABLET QD
126192353 12619235 2 SS FLAGYL METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE 1 Unknown U 0
126192353 12619235 3 C BABY ASPIRIN ASPIRIN 1 0
126192353 12619235 4 C ADCIRCA TADALAFIL 1 0
126192353 12619235 5 C TYVASO TREPROSTINIL 1 0
126192353 12619235 6 C PYRIDOXINE PYRIDOXINE 1 0
126192353 12619235 7 C LEVETIRACETAM. LEVETIRACETAM 1 0
126192353 12619235 8 C FUROSEMIDE. FUROSEMIDE 1 0
126192353 12619235 9 C DIASTAT ACUDIAL DIAZEPAM 1 0
126192353 12619235 10 C TUMS KIDS 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126192353 12619235 1 Pulmonary arterial hypertension
126192353 12619235 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126192353 12619235 HO
126192353 12619235 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126192353 12619235 Adenotonsillectomy
126192353 12619235 Arthritis reactive
126192353 12619235 Clostridium difficile infection
126192353 12619235 Joint swelling
126192353 12619235 Off label use

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

no results found

Therapies reported

no results found