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
126749072 12674907 2 F 20160111 20160119 20160822 20160913 PER US-RECKITT BENCKISER HEALTHCARE INT LIMITED-RB-81292-2016 RECKITT BENCKISER 69.00 YR F Y 0.00000 20160913 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
126749072 12674907 1 PS MUCINEX GUAIFENESIN 1 Unknown 1 DF, QD U U 0 1 DF
126749072 12674907 2 SS MUCINEX MAXIMUM STRENGTH GUAIFENESIN 1 Unknown 1200 MG, QD U U BD122 0 1200 MG TABLET
126749072 12674907 3 C PROZAC FLUOXETINE HYDROCHLORIDE 1 Unknown UNK U 0
126749072 12674907 4 C SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown UNK U 0
126749072 12674907 5 C AMLODIPIN /00972401/ AMLODIPINE BESYLATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126749072 12674907 1 Nasopharyngitis
126749072 12674907 2 Nasopharyngitis
126749072 12674907 3 Product used for unknown indication
126749072 12674907 4 Product used for unknown indication
126749072 12674907 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126749072 12674907 Aphonia
126749072 12674907 Condition aggravated
126749072 12674907 Cough
126749072 12674907 Glossodynia
126749072 12674907 Incorrect drug administration duration
126749072 12674907 Oropharyngeal pain
126749072 12674907 Swollen tongue

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
126749072 12674907 1 20160111 0
126749072 12674907 2 20160111 0