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
125487361 12548736 1 I 201605 20160628 20160712 20160712 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-42145BP BOEHRINGER INGELHEIM 78.58 YR F Y 39.00000 KG 20160712 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
125487361 12548736 1 PS MIRAPEX PRAMIPEXOLE DIHYDROCHLORIDE 1 Oral 0.75 MG Y 407716 22421 .75 MG TABLET QD
125487361 12548736 2 SS MIRAPEX PRAMIPEXOLE DIHYDROCHLORIDE 1 Oral 1.5 MG Y 407716 22421 .75 MG TABLET BID
125487361 12548736 3 C SELEGILINE SELEGILINE 1 Oral 10 MG 0 5 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125487361 12548736 1 Parkinson's disease
125487361 12548736 3 Parkinson's disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125487361 12548736 Blood pressure increased
125487361 12548736 Dysphonia
125487361 12548736 Eye disorder
125487361 12548736 Fatigue
125487361 12548736 Joint swelling
125487361 12548736 Medication error
125487361 12548736 Rhinorrhoea
125487361 12548736 Tongue movement disturbance
125487361 12548736 Weight increased

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
125487361 12548736 1 201603 201605 0
125487361 12548736 2 201605 20160626 0
125487361 12548736 3 201602 0