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
124065024 12406502 4 F 201511 20160801 20160526 20160803 EXP US-009507513-1605USA011019 MERCK 45.79 YR F Y 74.38000 KG 20160803 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
124065024 12406502 1 PS PRINIVIL LISINOPRIL 1 Oral 10 MG, QD U 19558 10 MG TABLET QD
124065024 12406502 2 C LYRICA PREGABALIN 1 Oral 50 MG (1 CAPSULE), TID U 0 50 MG CAPSULE TID
124065024 12406502 3 C THIOCTIC ACID THIOCTIC ACID 1 Oral 50 MG (1 TABLET), QD U 0 50 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124065024 12406502 1 Hypertension
124065024 12406502 2 Neuropathy peripheral

Outcome of event

Event ID CASEID OUTC COD
124065024 12406502 HO
124065024 12406502 OT
124065024 12406502 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
124065024 12406502 Allergic oedema
124065024 12406502 Anaphylactic reaction
124065024 12406502 Angioedema
124065024 12406502 Blood pressure diastolic increased
124065024 12406502 Blood pressure increased
124065024 12406502 Blood pressure systolic increased
124065024 12406502 Brain injury
124065024 12406502 Cirrhosis alcoholic
124065024 12406502 Dysphagia
124065024 12406502 Heart rate increased
124065024 12406502 Mouth swelling
124065024 12406502 Nail dystrophy
124065024 12406502 Oral disorder
124065024 12406502 Oropharyngeal pain
124065024 12406502 Sensory loss
124065024 12406502 Stomatitis
124065024 12406502 Throat lesion
124065024 12406502 Thrombocytopenia
124065024 12406502 Tremor

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
124065024 12406502 1 20151102 20151117 0
124065024 12406502 2 20151102 0