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
127587841 12758784 1 I 20160622 0 20160918 20160918 DIR US-FDA-350927 FDA-CTU 63.00 YR F N 62.10000 KG 20160918 N 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
127587841 12758784 1 PS RECLAST ZOLEDRONIC ACID 1 0
127587841 12758784 2 C ALPRAZOLOM 2 0
127587841 12758784 4 C INHALER UNSPECIFIED INGREDIENT 1 0
127587841 12758784 6 C LONG LASTING INHALER 2 0
127587841 12758784 8 C IBUPROFEN. IBUPROFEN 1 0
127587841 12758784 10 C TYLENOL ACETAMINOPHEN 1 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127587841 12758784 Blood pressure decreased
127587841 12758784 Bone pain
127587841 12758784 Dehydration
127587841 12758784 Influenza like illness
127587841 12758784 Insomnia
127587841 12758784 Movement disorder
127587841 12758784 Pain
127587841 12758784 Presyncope
127587841 12758784 Pyrexia
127587841 12758784 Vertigo
127587841 12758784 Vision blurred
127587841 12758784 Vomiting
127587841 12758784 Weight decreased

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

no results found

Therapies reported

no results found