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
92372532 9237253 2 F 201202 20160729 20130417 20160808 EXP US-009507513-1304USA007599 MERCK 0.00 F Y 0.00000 20160808 LW 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
92372532 9237253 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 10 MG, UNKNOWN U 20560 10 MG TABLET
92372532 9237253 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, UNK U 20560 70 MG TABLET
92372532 9237253 3 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, UNK U 20560 70 MG TABLET
92372532 9237253 4 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNK U 0 70 MG
92372532 9237253 5 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNK U 0 70 MG
92372532 9237253 6 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, UNK U 0 70 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92372532 9237253 1 Product used for unknown indication
92372532 9237253 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
92372532 9237253 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
92372532 9237253 Angina pectoris
92372532 9237253 Arthralgia
92372532 9237253 Drug ineffective
92372532 9237253 Femur fracture

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
92372532 9237253 1 200101 2001 0
92372532 9237253 2 200107 200301 0
92372532 9237253 3 200609 200707 0
92372532 9237253 4 200803 200905 0
92372532 9237253 5 201002 201007 0
92372532 9237253 6 201010 201112 0