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
6767311 7370573 F 6767311-6 20100329 20100601 20100614 EXP CH-CELGENEUS-151-C5013-10041417 CELGENEUS 73 YR M Y 68.7 KG 20100614 OT SWITZERLAND

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
6767311 1013856236 PS THALIDOMIDE 1 ORAL 060100
6767311 1013856237 SS THALIDOMIDE 1 ORAL 060100
6767311 1013856238 SS PREDNISONE 1 UNKNOWN
6767311 1013856239 SS PREDNISONE 1 UNKNOWN
6767311 1013856240 SS MELPHALAN HYDROCHLORIDE 1 UNKNOWN 060100
6767311 1013856241 SS MELPHALAN HYDROCHLORIDE 1 UNKNOWN 060100
6767311 1013856242 SS MORPHINE 1 ORAL
6767311 1013856243 SS MORPHINE 1 ORAL
6767311 1013856244 C NEXIUM 1 ORAL
6767311 1013856245 C NEXIUM 1 ORAL
6767311 1013856246 C TRAMAL 2 ORAL
6767311 1013856247 C TRAMAL 2 ORAL
6767311 1013856248 C MS CONTIN 1 ORAL
6767311 1013856249 C MS CONTIN 1 ORAL
6767311 1013856250 C MS CONTIN 1 ORAL
6767311 1013856251 C ZOMETA 1 PARENTERAL
6767311 1013856252 C SINTROM 1 UNKNOWN
6767311 1013856253 C CLEXANE 2 SUBCUTANEOUS
6767311 1013856254 C FRAXIFORTE 2 SUBCUTANEOUS
6767311 1013856255 C PRIMPERAN 2 ORAL
6767311 1013856256 C ZOFRAN 1 ORAL
6767311 1013856257 C DAFALGAN 2 ORAL
6767311 1013856258 C TOREM 2 ORAL
6767311 1013856259 C TOREM 2 ORAL
6767311 1013856260 C TOREM 2 ORAL
6767311 1013856261 C SORTIS 2 ORAL
6767311 1013856262 C NULYTELY 1 ORAL
6767311 1013856263 C LORAZEPAM 1 ORAL
6767311 1013856264 C BIPHOSPHONATE 2 UNKNOWN
6767311 1013856265 C KONAKION 1 ORAL
6767311 1013856266 C LMWH 2 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
6767311 1013856236 MULTIPLE MYELOMA
6767311 1013856238 MULTIPLE MYELOMA
6767311 1013856240 MULTIPLE MYELOMA
6767311 1013856242 BONE PAIN
6767311 1013856244 PROPHYLAXIS
6767311 1013856246 PAIN
6767311 1013856248 PAIN
6767311 1013856251 PROPHYLAXIS
6767311 1013856255 DRUG USE FOR UNKNOWN INDICATION
6767311 1013856256 DRUG USE FOR UNKNOWN INDICATION
6767311 1013856257 DRUG USE FOR UNKNOWN INDICATION
6767311 1013856258 DRUG USE FOR UNKNOWN INDICATION
6767311 1013856262 DRUG USE FOR UNKNOWN INDICATION
6767311 1013856263 DRUG USE FOR UNKNOWN INDICATION
6767311 1013856264 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
6767311 HO
6767311 OT

Reactions reported

Event ID PT
6767311 CONSTIPATION
6767311 DECREASED APPETITE
6767311 DEHYDRATION
6767311 GENERAL PHYSICAL HEALTH DETERIORATION

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
6767311 1013856236 20100315 20100412
6767311 1013856237 20100426
6767311 1013856238 20100315 20100318 6 DAY
6767311 1013856239 20100426 20100429 6 DAY
6767311 1013856240 20100315 20100318 6 DAY
6767311 1013856241 20100426 20100429 6 DAY
6767311 1013856242 20100322 20100325
6767311 1013856243 20100326
6767311 1013856244 20100315 20100415
6767311 1013856245 20100420
6767311 1013856246 20100308 20100322
6767311 1013856247 20100307
6767311 1013856248 20100322 20100325
6767311 1013856249 20100326 20100425
6767311 1013856250 20100426
6767311 1013856251 20100308
6767311 1013856252 20100416
6767311 1013856253 20100416 20100421 5 DAY
6767311 1013856254 20100422
6767311 1013856255 20100315
6767311 1013856256 20100315
6767311 1013856257 20100325
6767311 1013856258 20100411
6767311 1013856259 20100412 20100414
6767311 1013856260 20100416
6767311 1013856262 20100406 20100415 9 DAY
6767311 1013856263 20100416
6767311 1013856264 20100308