The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6252168 6356810 F 6252168-2 20070926 20090615 20090630 EXP GB-MERCK-0707USA01286 MERCK HUMAN HEALTH DIVISION 70 YR M Y 20090630 OT UNITED KINGDOM

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6252168 1011820324 PS PRINIVIL 1 ORAL 19558
6252168 1011820325 SS LIDOCAINE HYDROCHLORIDE 2 TOPICAL
6252168 1011820326 C PHENYLEPHRINE 2 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
6252168 1011820324 HYPERTENSION
6252168 1011820325 LOCAL ANAESTHESIA

Outcome of event

Event ID OUTC COD
6252168 HO
6252168 LT

Reactions reported

Event ID PT
6252168 ANGIOEDEMA
6252168 CONVULSION
6252168 DRUG HYPERSENSITIVITY
6252168 HYPOGLYCAEMIA
6252168 HYPOXIA
6252168 LARYNGEAL STENOSIS
6252168 OBSTRUCTIVE AIRWAYS DISORDER
6252168 OEDEMA
6252168 OEDEMA MUCOSAL
6252168 PALLOR
6252168 PULSE ABSENT
6252168 RENAL FAILURE ACUTE
6252168 RESPIRATORY ARREST
6252168 RESTLESSNESS
6252168 SWOLLEN TONGUE

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6252168 1011820324 6 MON