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
125534901 12553490 1 I 201509 20151022 20160713 20160713 PER US-PERRIGO-15US011175 PERRIGO 48.00 YR F Y 81.63000 KG 20160713 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
125534901 12553490 1 PS LANSOPRAZOLE. LANSOPRAZOLE 1 Oral 15 MG, QD U 5CE1430 202319 15 MG MODIFIED-RELEASE CAPSULE, HARD
125534901 12553490 2 C QNASL BECLOMETHASONE DIPROPIONATE 1 Nasal UNK U UNKNOWN 0
125534901 12553490 3 C CLARITIN LORATADINE 1 Oral UNK U UNKNOWN 0
125534901 12553490 4 C FLOVENT FLUTICASONE PROPIONATE 1 Oral UNK U UNKNOWN 0
125534901 12553490 5 C PEPCID /06376601/ 2 Oral UNKNOWN, EVERY MORNING U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125534901 12553490 1 Gastrooesophageal reflux disease
125534901 12553490 2 Seasonal allergy
125534901 12553490 3 Seasonal allergy
125534901 12553490 4 Eosinophilic oesophagitis
125534901 12553490 5 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125534901 12553490 Condition aggravated
125534901 12553490 Drug ineffective
125534901 12553490 Incorrect drug administration duration
125534901 12553490 Sensation of foreign body
125534901 12553490 Wrong technique in product usage process

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
125534901 12553490 1 201509 0