UNEVALUABLE EVENT side effect
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Drugs associated with UNEVALUABLE EVENT
ABILIFY ACTOS ALAVERT ALBUTEROL ALESSE ALEVE ALTACE AMLODIPINE ANDRODERM ANTABUSE ANTERIOR ARANESP ARIMIDEX ASMANEX ASPIRIN ATENOLOL ATIVAN ATROPINE AVASTIN AVELOX AVINZA AVONEX BACLOFEN BENADRYL BENICAR BETASERON BEVACIZUMAB BONE BOTOX BUMETANIDE BYETTA CAMPRAL CAMPTOSAR CEDAX CELEXA CHANTIX CIPROFLOXACIN CISPLATIN CITALOPRAM CLARITHROMYCIN CLIMARA COMPAZINE COZAAR CREST CRESTOR CYMBALTA DAYTRANA DEPAKENE DEPAKOTE DEXEDRINE DIGITEK DIGOXIN DILANTIN DILAUDID DILTIAZEM DOTAREM DURAGESIC DURAPREP EFFEXOR ENALAPRIL EPREX ERYTHROMYCIN EVISTA EXENATIDE FABRAZYME FENTANYL FINASTERIDE FLUOXETINE FLURAZEPAM FOCALIN FRONTAL FUROSEMIDE FUZEON GABAPENTIN GENOTROPIN GLUCOTROL HEPARIN HUMIRA HYDROCHLOROTHIAZ HYTRIN IBUPROFEN IMODIUM INTRON IPRATROPIUM ISOPTIN JANUVIA KALETRA KETEK LAMICTAL LANOXIN LEUPLINFORECTION LEVAQUIN LEVITRA LIPITOR LISINOPRIL LITHIUM LOTREL LOVENOX LUCENTIS LYRICA MABTHERA MACROBID MAGNEVIST MEDROL METHADONE METOPROLOL MIDOL MIFEPRISTONE MIRENA MOBIC MORPHINE MOXIFLOXACIN NARDIL NATALIZUMAB NEUPRO NEURONTIN NEXAVAR NEXIUM NIACIN NORDITROPIN NORVASC NUVARING OCTREOTIDE OMALIZUMAB OMNISCAN ORENCIA ORTHO OXYCONTIN PACLITAXEL PANTOPRAZOLE PAROXETINE PERCOCET PIMOZIDE PLAVIX PRAVASTATIN PREDNISONE PRILOSEC PROPAFENONE PROTONIX PROZAC QUININE RAPTIVA REBIF REDUCTIL REMERON REMICADE REVLIMID RIBAVIRIN RISPERDAL ROACCUTAN ROACUTAN ROCEPHIN ROZEREM SAMARIUM SAQUINAVIR SEMITENDINOSUS SEPTOCAINE SEROQUEL SEROSTIM SERTRALINE SIMVASTATIN SINGULAIR SORIATANE SOTALOL TAXOTERE TEKTURNA TEMOZOLOMIDE TERAZOSIN TESTIM THALOMID TIGAN TRAMADOL TRANSDERM TRAZODONE TREVILOR TRIAZOLAM TYSABRI ULTRAVIST VANCOMYCIN VARENICLINE VENLAFAXINE VERSED VIAGRA VINCRISTINE VIRACEPT VYTORIN WARFARIN WELCHOL WELLBUTRIN XOLAIR ZELDOX ZETIA ZEVALIN ZOCOR ZOLINZA ZOLOFT ZOLPIDEM ZOMETA ZYRTECHumira 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Mobic Side Effects Report #5637879-1
MOBIC problem was reported by a Consumer or non-health professional from UNITED STATES 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.
Fentanyl Side Effects Report #5639876-9
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem 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.
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.
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.
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.
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.
Cedax Side Effects Report #5585147-9
CEDAX problem was reported by a Consumer or non-health professional from UNITED STATES 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.
Fentanyl Side Effects Report #5588306-4
Pharmacist from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem 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.
Hytrin Side Effects Report #5591231-6
HYTRIN problem was reported by a Consumer or non-health professional from UNITED STATES 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.
Remicade Side Effects Report #5602274-8
Physician from UNITED STATES reported REMICADE problem 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.
Benadryl Side Effects Report #5603203-3
BENADRYL ALLERGY DYE problem was reported by a Consumer or non-health professional from UNITED STATES 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.
Temozolomide Side Effects Report #5605462-X
Consumer or non-health professional from UNITED STATES reported TEMOZOLOMIDE problem on Jan 24, 2008. Female patient, weighting 134.5 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . TEMOZOLOMIDE dosage: 875 MG. Patient recovered.
Vincristine Side Effects Report #5607281-7
VINCRISTINE problem was reported by a Consumer or non-health professional from GERMANY on Jan 16, 2008. Male patient, 56 years of age, was diagnosed with diffuse large b-cell lymphoma and was treated with VINCRISTINE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . VINCRISTINE dosage: unknown. During the same period patient was treated with ETOPOSIDE, DOXORUBICIN, CYCLOPHOSPHAMIDE, PREDNISONE. Patient recovered.
Vincristine Side Effects Report #5607598-6
Consumer or non-health professional from GERMANY reported VINCRISTINE problem on Jan 16, 2008. Male patient, 54 years of age, was diagnosed with non-hodgkin's lymphoma stage iii and was treated with VINCRISTINE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . VINCRISTINE dosage: unknown. During the same period patient was treated with ETOPOSIDE, DOXORUBICIN, CYCLOPHOSPHAMIDE, RITUXIMAB. Patient recovered.
Vincristine Side Effects Report #5607619-0
VINCRISTINE problem was reported by a Consumer or non-health professional from GERMANY on Jan 16, 2008. Female patient, 47 years of age, was diagnosed with diffuse large b-cell lymphoma and was treated with VINCRISTINE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . VINCRISTINE dosage: unknown. During the same period patient was treated with ETOPOSIDE, DOXORUBICIN, CYCLOPHOSPHAMIDE, PREDNISONE. Patient recovered.
Vincristine Side Effects Report #5607628-1
Consumer or non-health professional from GERMANY reported VINCRISTINE problem on Jan 16, 2008. Male patient, 52 years of age, was diagnosed with diffuse large b-cell lymphoma and was treated with VINCRISTINE. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . VINCRISTINE dosage: unknown. During the same period patient was treated with ETOPOSIDE, DOXORUBICIN, CYCLOPHOSPHAMIDE, RITUXIMAB. Patient recovered.
Aleve Side Effects Report #5609659-4
ALEVE COLD AND SINUS problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 07, 2007. Female patient, child 5 years of age, weighting 33.07 lb, was diagnosed with accidental exposure and was treated with ALEVE COLD AND SINUS. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE COLD AND SINUS dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. Patient recovered.
Aleve Side Effects Report #5609662-4
Consumer or non-health professional from UNITED STATES reported ALEVE COLD AND SINUS problem on Dec 14, 2006. Male patient, 15 years of age, weighting 114.6 lb, was treated with ALEVE COLD AND SINUS. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE COLD AND SINUS dosage: TOTAL DAILY DOSE: 440 MG UNIT DOSE: 220 MG. Patient recovered.
Aleve Side Effects Report #5609674-0
ALEVE COLD AND SINUS problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 25, 2007. Female patient, 30 years of age, weighting 130.1 lb, was diagnosed with sinus congestion and was treated with ALEVE COLD AND SINUS. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE COLD AND SINUS dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. During the same period patient was treated with YASMIN. Patient recovered.
Aleve Side Effects Report #5609692-2
Consumer or non-health professional from UNITED STATES reported ALEVE COLD AND SINUS problem on Mar 30, 2007. Female patient, weighting 145.5 lb, was treated with ALEVE COLD AND SINUS. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE COLD AND SINUS dosage: UNIT DOSE: 220 MG. Patient recovered.
Aleve Side Effects Report #5609727-7
ALEVE COLD AND SINUS problem was reported by a Consumer or non-health professional from UNITED STATES on June 27, 2007. Male patient, 29 years of age, weighting 165.3 lb, was treated with ALEVE COLD AND SINUS. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE COLD AND SINUS dosage: TOTAL DAILY DOSE: 440 MG UNIT DOSE: 220 MG. Patient recovered.
Aleve Side Effects Report #5609734-4
Consumer or non-health professional from UNITED STATES reported ALEVE COLD AND SINUS problem on Dec 19, 2006. Female patient, 17 years of age, weighting 99.21 lb, was treated with ALEVE COLD AND SINUS. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE COLD AND SINUS dosage: TOTAL DAILY DOSE: 220 MG UNIT DOSE: 220 MG. During the same period patient was treated with ALEVE COLD AND SINUS. Patient recovered.
Aleve Side Effects Report #5609740-X
ALEVE COLD AND SINUS problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 04, 2007. Male patient, 22 years of age, weighting 141.1 lb, was treated with ALEVE COLD AND SINUS. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE COLD AND SINUS dosage: AS USED: 440/240 MG UNIT DOSE: 440 MG. Patient recovered.
Aleve Side Effects Report #5609741-1
Consumer or non-health professional from UNITED STATES reported ALEVE COLD AND SINUS problem on Mar 10, 2007. Male patient, 28 years of age, weighting 216.1 lb, was treated with ALEVE COLD AND SINUS. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE COLD AND SINUS dosage: UNIT DOSE: 220 MG. Patient recovered.
Aleve Side Effects Report #5609749-6
ALEVE COLD AND SINUS problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 16, 2007. Female patient, child 3 years of age, weighting 39.68 lb, was diagnosed with accidental exposure, hypersensitivity and was treated with ALEVE COLD AND SINUS. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE COLD AND SINUS dosage: AS USED: 220/120 MG UNIT DOSE: 220 MG. During the same period patient was treated with EQUATE SINUS. Patient recovered.
Aleve Side Effects Report #5609796-4
Consumer or non-health professional from UNITED STATES reported ALEVE COLD AND SINUS problem on Oct 25, 2007. Female patient, 26 years of age, weighting 125.7 lb, was diagnosed with endodontic procedure and was treated with ALEVE COLD AND SINUS. After drug was administered, patient experienced the following problems/side effects: unevaluable event, . ALEVE COLD AND SINUS dosage: unknown. During the same period patient was treated with VICODIN. Patient recovered.