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
126561271 12656127 1 I 201608 20160812 20160816 20160816 PER US-BAYER-2016-157726 BAYER 78.00 YR E F Y 50.80000 KG 20160816 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
126561271 12656127 1 PS CLARITIN-D 12 HOUR LORATADINEPSEUDOEPHEDRINE SULFATE 1 Oral 1 DF, QD Y CVM05N8 19670 1 DF PROLONGED-RELEASE TABLET QD
126561271 12656127 2 C ASPIRIN. ASPIRIN 1 UNK 0
126561271 12656127 3 C STATIN UNSPECIFIED INGREDIENT 1 UNK 0
126561271 12656127 4 C SYNTHROID LEVOTHYROXINE SODIUM 1 UNK 0
126561271 12656127 5 C LOVAZA OMEGA-3-ACID ETHYL ESTERS 1 UNK 0
126561271 12656127 6 C VASOGEN 2 0
126561271 12656127 7 C COQ10 UBIDECARENONE 1 UNK 0
126561271 12656127 8 C CALCIUM CALCIUM 1 UNK 0
126561271 12656127 9 C VITAMIN D3 CHOLECALCIFEROL 1 UNK 0
126561271 12656127 10 C VITAMIN C ASCORBIC ACID 1 0
126561271 12656127 11 C LUTEIN LUTEIN 1 0
126561271 12656127 12 C MULTIVITAMIN VITAMINS 1 UNK 0
126561271 12656127 13 C MAGNESIUM MAGNESIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126561271 12656127 1 Upper-airway cough syndrome
126561271 12656127 2 Ischaemic heart disease prophylaxis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126561271 12656127 Drug prescribing error
126561271 12656127 Insomnia
126561271 12656127 Product use issue

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
126561271 12656127 1 20160808 20160811 0