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
8554345 8695088 I 8554345-4 20120723 20120731 EXP US-009507513-1207USA009796 MERCK AND CO INC YR Y 20120731 OT UNITED STATES

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
8554345 1020405358 PS ZOCOR 1 ORAL 019766
8554345 1020405360 SS ZANTAC 1
8554345 1020405362 SS METHOCARBAMOL 1 ORAL
8554345 1020405363 SS ISOSORBIDE MONONITRATE 1
8554345 1020405372 SS NITROSTAT 1
8554345 1020405376 SS DILANTIN 1 ORAL
8554345 1020405371 SS REMERON 1 ORAL
8554345 1020405364 SS POTASSIUM CHLORIDE 1
8554345 1020405365 SS DEPAKOTE 1 ORAL
8554345 1020405369 SS LANTUS 1 90 DF, QPM
8554345 1020405373 SS ATENOLOL 1 ORAL
8554345 1020405374 SS ATIVAN 1 ORAL
8554345 1020405367 SS FUROSEMIDE 1 ORAL
8554345 1020405375 SS NORVASC 1 ORAL
8554345 1020405370 SS GENERLAC 1
8554345 1020405359 SS TYLENOL W/ CODEINE NO. 3 1
8554345 1020405361 SS LOMOTIL 1 ORAL
8554345 1020405366 SS HUMULIN R 1
8554345 1020405377 SS ASPIRIN 1
8554345 1020405368 SS LANTUS 1 80 IU, QAM

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
8554345 OT
8554345 DS

Reactions reported

Event ID PT
8554345 CHRONIC OBSTRUCTIVE PULMONARY DISEASE
8554345 BEDRIDDEN
8554345 EMPHYSEMA
8554345 AMNESIA

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

no results found

Therapies reported

no results found