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
127428971 12742897 1 I 20160911 0 20160914 20160914 DIR US-FDA-350571 FDA-CTU 52.00 YR F N 77.40000 KG 20160914 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
127428971 12742897 1 PS COMPAZINE PROCHLORPERAZINE MALEATE 1 Intravenous (not otherwise specified) N D 0
127428971 12742897 2 C LEVOTHYROXIN LEVOTHYROXINE 1 0
127428971 12742897 3 C SIMVASTATIN. SIMVASTATIN 1 0
127428971 12742897 5 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 0
127428971 12742897 7 C SINGULAIR MONTELUKAST SODIUM 1 0
127428971 12742897 9 C VITAMINS VITAMINS 1 0
127428971 12742897 11 C BIOTIN BIOTIN 1 0
127428971 12742897 13 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0
127428971 12742897 15 C MUCINEX GUAIFENESIN 1 0
127428971 12742897 17 C PROBIOTIC PROBIOTICS NOS 1 0
127428971 12742897 19 C MAGNESIUM MAGNESIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127428971 12742897 1 Headache

Outcome of event

Event ID CASEID OUTC COD
127428971 12742897 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127428971 12742897 Chest discomfort
127428971 12742897 Contraindicated product administered
127428971 12742897 Dyspnoea
127428971 12742897 Panic reaction
127428971 12742897 Swelling face

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
127428971 12742897 1 20160911 20160911 0