UNEVALUABLE EVENT side effect
What is UNEVALUABLE EVENT ?Drugs associated with UNEVALUABLE EVENT
ABILIFY ALEVE AMLODIPINE ANDRODERM ANGELIQ ANTERIOR APIDRA ARIMIDEX ARTHROTEC ASPIRIN AVASTIN AVELOX AVINZA AVONEX BENADRYL BENICAR BETASERON BONE BOTOX BUMETANIDE BYETTA CANCELLOUS CEDAX CELEXA CELLCEPT CHANTIX CITALOPRAM CLARITHROMYCIN CLIMARA COLESTIPOL COLLOIDAL CRESTOR DEPAKENE DILANTIN DILAUDID DILTIAZEM DURAGESIC DURAPREP EFFEXOR EMSAM ENALAPRIL ENBREL EVISTA EXENATIDE FENTANYL FLOXIN FLUOXETINE FOCALIN FUROSEMIDE FUZEON GABAPENTIN GEODON HEPARIN HUMIRA HYDROCHLOROTHIAZ HYTRIN IBUPROFEN INTRON INVIRASE IPRATROPIUM ISOPTIN JANUVIA KALETRA LEVAQUIN LEVITRA LIPITOR LITHIUM LUCENTIS LYRICA MACROBID MAGNEVIST METOPROLOL MIDOL MIRENA MOBIC MORPHINE NEURONTIN NEXAVAR NORDITROPIN NORVASC OCTREOTIDE OMALIZUMAB ORENCIA ORTHO OXYCONTIN PACLITAXEL PAROXETINE PERCOCET PIMOZIDE PRECOSE PREGABALIN PROPAFENONE PROZAC RAPTIVA REBIF REDUCTIL REMERON REMICADE REVLIMID RIBAVIRIN ROACUTAN ROCEPHIN ROZEREM SAQUINAVIR SEROQUEL SERTRALINE SILVADENE SINGULAIR SPIRIVA SUTENT SYNTHROID TEKTURNA TEMOZOLOMIDE THALOMID TIKOSYN TRASYLOL TREVILOR TRIAZOLAM TYSABRI ULTRAVIST VANCOMYCIN VENLAFAXIINE VENLAFAXINE VERSED VESICARE VIAGRA VINCRISTINE VYTORIN WARFARIN WELLBUTRIN XOLAIR ZEVALIN ZOCOR ZOLPIDEM ZOSYN ZYRTECUNEVALUABLE EVENT : Humira Side Effects Report #5647616-2
Consumer or non-health professional from CANADA reported HUMIRA problem on Feb 22, 2008. Female patient, weighting 130.1 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . HUMIRA dosage: unknown. Patient was hospitalized. Patient recovered.
UNEVALUABLE EVENT : Aleve Side Effects Report #5656306-1
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 11, 2007. Male patient, 23 years of age, weighting 134.5 lb, was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Aleve Side Effects Report #5656383-8
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Dec 14, 2007. Male patient, 58 years of age, weighting 200.6 lb, was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE dosage: unknown. During the same period patient was treated with EQUATE ASPIRIN. Patient recovered.
UNEVALUABLE EVENT : Aleve Side Effects Report #5659074-2
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 29, 2007. Female patient was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. Patient recovered.
UNEVALUABLE EVENT : Aleve Side Effects Report #5659156-5
Consumer or non-health professional from UNITED STATES reported ALEVE problem on May 23, 2007. Female patient, 30 years of age, weighting 200.6 lb, was diagnosed with accidental exposure and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE dosage: TOTAL DAILY DOSE: 880 MG UNIT DOSE: 220 MG. Patient recovered.
UNEVALUABLE EVENT : Midol Side Effects Report #5659157-7
MIDOL problem was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2007. Female patient, 20 years of age, weighting 125.7 lb, was treated with MIDOL. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . MIDOL dosage: UNIT DOSE: 220 MG. Patient recovered.
UNEVALUABLE EVENT : Aleve Side Effects Report #5659165-6
Consumer or non-health professional from UNITED STATES reported ALEVE problem on May 22, 2007. Female patient, child 2 years of age, weighting 33.07 lb, was diagnosed with accidental exposure and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE dosage: unknown. During the same period patient was treated with PULMICORT, NASONEX, SINGULAIR. Patient recovered.
UNEVALUABLE EVENT : Aleve Side Effects Report #5659168-1
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on June 03, 2007. Male patient, 18 years of age, weighting 169.8 lb, was diagnosed with accidental overdose and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE dosage: TOTAL DAILY DOSE: 880 MG UNIT DOSE: 220 MG. Patient recovered.
UNEVALUABLE EVENT : Aleve Side Effects Report #5659231-5
Consumer or non-health professional from UNITED STATES reported ALEVE problem on June 08, 2007. Female patient, 67 years of age, weighting 149.9 lb, was diagnosed with accidental overdose and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with HYZAAR, SYNTHROID, IMIPRAMINE. Patient recovered.
UNEVALUABLE EVENT : Aleve Side Effects Report #5659259-5
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on June 17, 2007. Male patient, child 2 years of age, weighting 26.46 lb, was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Heparin Side Effects Report #5661179-7
Consumer or non-health professional from UNITED STATES reported HEPARIN problem on Mar 12, 2008. Male patient, 40 years of age, weighting 190.0 lb, was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . HEPARIN dosage: unknown. Patient died on 12/10/2007.
UNEVALUABLE EVENT : Humira Side Effects Report #5667867-0
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 04, 2008. Female patient, 41 years of age, was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . HUMIRA dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Percocet Side Effects Report #5674801-6
Consumer or non-health professional from UNITED STATES reported PERCOCET problem on Mar 19, 2008. Female patient, 62 years of age, was diagnosed with pain and was treated with PERCOCET. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . PERCOCET dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Avonex Side Effects Report #5680998-4
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 11, 2008. Male patient was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . AVONEX dosage: unknown. Patient died.
UNEVALUABLE EVENT : Mirena Side Effects Report #5687294-X
Physician from UNITED STATES reported MIRENA problem on Jan 25, 2007. Female patient was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . MIRENA dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Avelox Side Effects Report #5688517-3
AVELOX problem was reported by a Health Professional from UNITED STATES on Mar 18, 2008. Male patient was diagnosed with respiratory tract infection and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . AVELOX dosage: unknown. Patient was hospitalized. Patient recovered.
UNEVALUABLE EVENT : Singulair Side Effects Report #5690418-1
Health Professional from UNITED STATES reported SINGULAIR problem on Mar 31, 2008. Female patient, 44 years of age, weighting 166.0 lb, was diagnosed with rhinitis allergic and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . SINGULAIR dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Orencia Side Effects Report #5690654-4
ORENCIA problem was reported by a Pharmacist from UNITED STATES on Mar 31, 2008. Female patient, 74 years of age, weighting 165.0 lb, was diagnosed with rheumatoid arthritis and was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ORENCIA dosage: 750MG EVERY TWO WEEKS IV DRIP. Patient was hospitalized. Patient recovered.
UNEVALUABLE EVENT : Thalomid Side Effects Report #5618540-6
Consumer or non-health professional from UNITED STATES reported THALOMID problem on Jan 24, 2008. Male patient, 84 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . THALOMID dosage: 200 MG, 1 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.
UNEVALUABLE EVENT : Lipitor Side Effects Report #5619553-0
LIPITOR problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 05, 2008. Male patient, 55 years of age, weighting 185.0 lb, was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . LIPITOR dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Avelox Side Effects Report #5620585-7
Pharmacist from UNITED STATES reported AVELOX problem on Jan 08, 2008. Female patient was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . AVELOX dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Magnevist Side Effects Report #5624120-9
MAGNEVIST problem was reported by a Physician from CANADA on Feb 06, 2008. Female patient was diagnosed with nuclear magnetic resonance imaging and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . MAGNEVIST dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Fentanyl Side Effects Report #5624460-3
Physician from UNITED STATES reported FENTANYL problem on Jan 25, 2008. Female patient, 56 years of age, was treated with FENTANYL. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . FENTANYL dosage: unknown. During the same period patient was treated with HYDROCODONE BITARTRATE AND ACETAMINOPHEN, OXYCODONE, CARISOPRODOL, DIPHENHYDRAMINE, ACETAMINOPHEN IN COMBINATION, CITALOPRAM HYDROBROMIDE, BUPROPION, TRAZODONE. Patient died.
UNEVALUABLE EVENT : Zocor Side Effects Report #5626181-X
ZOCOR problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 13, 2008. Female patient, weighting 138.0 lb, was diagnosed with blood cholesterol abnormal and was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ZOCOR dosage: * 40 MG 1/2 TAB DAILY ORAL. Patient recovered.
UNEVALUABLE EVENT : Climara Side Effects Report #5626342-X
Physician from UNITED STATES reported CLIMARA problem on Feb 12, 2008. Female patient was diagnosed with menopausal disorder and was treated with CLIMARA. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . CLIMARA dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Gabapentin Side Effects Report #5628689-X
GABAPENTIN problem was reported by a Pharmacist from UNITED STATES on Feb 15, 2008. Male patient, 59 years of age, was treated with GABAPENTIN. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . GABAPENTIN dosage: 300MG TID ORAL. Patient recovered.
UNEVALUABLE EVENT : Focalin Side Effects Report #5629498-8
Health Professional from UNITED STATES reported FOCALIN problem on Feb 15, 2008. Male patient, weighting 115.7 lb, was diagnosed with attention deficit/hyperactivity disorder, bipolar disorder and was treated with FOCALIN. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . FOCALIN dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Avonex Side Effects Report #5631029-3
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2008. Male patient, 47 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
UNEVALUABLE EVENT : Avastin Side Effects Report #5633947-9
Consumer or non-health professional from UNITED STATES reported AVASTIN problem on Feb 14, 2008. Male patient was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . AVASTIN dosage: unknown. Patient was hospitalized. Patient recovered.
UNEVALUABLE EVENT : Floxin Side Effects Report #5636088-X
FLOXIN problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 15, 2008. Female patient was treated with FLOXIN. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . FLOXIN dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Mobic Side Effects Report #5637879-1
Consumer or non-health professional from UNITED STATES reported MOBIC problem on Feb 25, 2008. Female patient, weighting 200.0 lb, was diagnosed with osteoarthritis and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . MOBIC dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Fentanyl Side Effects Report #5639876-9
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 18, 2008. Female patient, weighting 114.0 lb, was diagnosed with gout, pain, thyroidectomy, restless legs syndrome, depression, pneumonia and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with MORPHINE, METOPROLOL TARTRATE, XANAX, SYNTHROID, OMEPRAZOLE, REQUIP, PAXIL, COMBIVENT. Patient died on 02/01/2008.
UNEVALUABLE EVENT : Duragesic Side Effects Report #5642451-3
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Feb 20, 2008. Male patient was diagnosed with cancer pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . DURAGESIC dosage: unknown. Patient died on 05/01/2007.
UNEVALUABLE EVENT : Levitra Side Effects Report #5645209-4
LEVITRA problem was reported by a Health Professional from UNITED STATES on Jan 31, 2008. Male patient was treated with LEVITRA. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . LEVITRA dosage: TOTAL DAILY DOSE: 10 MG UNIT DOSE: 10 MG. Patient recovered.
UNEVALUABLE EVENT : Avelox Side Effects Report #5646513-6
Pharmacist from UNITED STATES reported AVELOX problem on Feb 28, 2008. Male patient, weighting 215.0 lb, was diagnosed with upper respiratory tract infection and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . AVELOX dosage: unknown. During the same period patient was treated with ACTOS, ALTACE, TOPROL, LIPITOR, EFFEXOR, AMBIEN, LORAZEPAM. Patient was hospitalized. Patient recovered.
UNEVALUABLE EVENT : Januvia Side Effects Report #5656585-0
JANUVIA problem was reported by a Health Professional from UNITED STATES on Dec 20, 2007. Female patient was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . JANUVIA dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Lithium Side Effects Report #5583978-2
Pharmacist from UNITED STATES reported LITHIUM CARBONATE problem on Jan 03, 2008. Male patient, 50 years of age, weighting 220.5 lb, was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . LITHIUM CARBONATE dosage: 450 MG BID PO. Patient recovered.
UNEVALUABLE EVENT : Remicade Side Effects Report #5584414-2
REMICADE problem was reported by a Physician from UNITED KINGDOM on Jan 02, 2008. Female patient was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . REMICADE dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Cedax Side Effects Report #5585147-9
Consumer or non-health professional from UNITED STATES reported CEDAX problem on Jan 04, 2008. Female patient was diagnosed with ear disorder, respiratory tract infection, sinus disorder, cough and was treated with CEDAX. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . CEDAX dosage: unknown. During the same period patient was treated with CEFDINIR. Patient recovered.
UNEVALUABLE EVENT : Fentanyl Side Effects Report #5588306-4
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Pharmacist from UNITED STATES on Dec 27, 2007. Male patient, weighting 110.2 lb, was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. Patient was hospitalized. Patient recovered.
UNEVALUABLE EVENT : Avelox Side Effects Report #5589333-3
Consumer or non-health professional from UNITED STATES reported AVELOX problem on Dec 14, 2007. Female patient was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . AVELOX dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Hytrin Side Effects Report #5591212-2
HYTRIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 31, 2007. Female patient was treated with HYTRIN. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . HYTRIN dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Hytrin Side Effects Report #5591231-6
Consumer or non-health professional from UNITED STATES reported HYTRIN problem on July 05, 2007. Male patient, 85 years of age, was treated with HYTRIN. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . HYTRIN dosage: unknown. During the same period patient was treated with ALFUZOSIN HYDROCHLORIDE. Patient recovered.
UNEVALUABLE EVENT : Aleve Side Effects Report #5593750-5
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 11, 2007. Female patient was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Spiriva Side Effects Report #5593789-X
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Dec 20, 2007. Male patient was diagnosed with chronic obstructive pulmonary disease, emphysema, dyspnoea and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . SPIRIVA dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Tikosyn Side Effects Report #5595349-3
TIKOSYN problem was reported by a Physician from UNITED STATES on Jan 09, 2008. Female patient was treated with TIKOSYN. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . TIKOSYN dosage: unknown. Patient was hospitalized. Patient recovered.
UNEVALUABLE EVENT : Precose Side Effects Report #5596998-9
Consumer or non-health professional from UNITED STATES reported PRECOSE problem on Dec 19, 2007. Female patient was treated with PRECOSE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . PRECOSE dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Magnevist Side Effects Report #5599480-8
MAGNEVIST problem was reported by a Health Professional from UNITED STATES on Jan 17, 2008. Male patient was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . MAGNEVIST dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Mirena Side Effects Report #5600838-9
Health Professional from UNITED STATES reported MIRENA problem on Jan 11, 2008. Female patient was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . MIRENA dosage: unknown. Patient recovered.
UNEVALUABLE EVENT : Remicade Side Effects Report #5602274-8
REMICADE problem was reported by a Physician from UNITED STATES on Jan 18, 2008. Female patient, weighting 224.0 lb, was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.
UNEVALUABLE EVENT : Benadryl Side Effects Report #5603203-3
Consumer or non-health professional from UNITED STATES reported BENADRYL ALLERGY DYE problem on Jan 10, 2008. Female patient was diagnosed with hypersensitivity and was treated with BENADRYL ALLERGY DYE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . BENADRYL ALLERGY DYE dosage: unknown. Patient recovered.