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CONDITION AGGRAVATED side effect

What is CONDITION AGGRAVATED ?
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Drugs associated with CONDITION AGGRAVATED

ABACAVIR  ABELCET  ABRAXANE  ACETAMINOPHEN  ACETAZOLAMIDE  ACETYLSALICYLIC  ACIPHEX  ACITRETIN  ACTIQ  ACTIVASE  ACTONEL  ACTOS  ACYCLOVIR  ADALIMUMAB  ADDERALL  ADVAIR  ADVIL  AFRIN  ALAWAY  ALBENDAZOLE  ALBUTEROL  ALDARA  ALDURAZYME  ALESION  ALEVE  ALIMTA  ALLEGRA  ALLOPURINOL  ALPRAZOLAM  ALTABAX  ALTACE  AMBIEN  AMBISOME  AMEVIVE  AMIODARONE  AMITIZA  AMLODIPINE  AMOXICILLIN  AMOXIL  ANADIN  ANANDRON  APLISOL  APOKYN  ARAVA  ARICEPT  ARIMIDEX  ARIPIPRAZOLE  ARIXTRA  AROMASIN  ARSENIC  ARTHROTEC  ASACOL  ASPIRIN  ATHLETES  ATIVAN  ATLANSIL  AUGMENTIN  AVANDAMET  AVANDIA  AVASTIN  AVEENO  AVELOX  AVODART  AVONEX  AZASAN  AZATHIOPRINE  AZILECT  AZITHROMYCIN  AZOPT  AZULFIDINE  BCG  BECLOMETHASONE  BECONASE  BENADRYL  BENZOYL  BETAMETHASONE  BETASERON  BEVACIZUMAB  BEXTRA  BIAXIN  BISOPROLOL  BONIVA  BOTOX  BOTULINUM  BROVANA  BUDEPION  BUDEPRION  BUDIPRION  BUPIVACAINE  BUPROPION  BUSPIRONE  BYETTA  CABASERIL  CABERGOLINE  CALCIUM  CANCIDAS  CAP  CARBAMAZEPINE  CARBIDOPA  CARBOPLATIN  CARDIZEM  CARVEDILOL  CEFDITOREN  CEFTAZIDIME  CEFTRIAXONE  CEFUROXIME  CELEBREX  CELEXA  CENESTIN  CENTRUM  CEPHALEXIN  CEREZYME  CESAMET  CHAMPIX  CHANTIX  CIFLOX  CILOSTAZOL  CIPROFLOXACIN  CISPLATIN  CITALOPRAM  CLARAVIS  CLARITHROMYCIN  CLARITIN  CLAVAMOX  CLEMASTINE  CLINDAMYCIN  CLOBETASOL  CLOFARABINE  CLONAZEPAM  CLONIDINE  CLOZAPIN  CLOZAPINE  CLOZARIL  COAPROVEL  COLAZAL  COLISTIN  COMBIVENT  COMMIT  COMPETACT  COMTAN  COOLMETEC  COPAXONE  CORDARONE  COREG  COROTROPE  COTRIM  COZAAR  CRESTOR  CROMOLYN  CUBICIN  CYCLOPHOSPHAMIDE CYCLOSPORINE  CYMBALTA  CYTARABINE  DACLIZUMAB  DACOGEN  DACTINOMYCIN  DAIVOBET  DALTEPARIN  DAPSONE  DECADRON  DECITABINE  DESLORATADINE  DESOXIMETASONE  DIABEX  DIAMOX  DIANEAL  DIAZEPAM  DICLOFENAC  DIDANOSINE  DIDRONEL  DIGOXIN  DIHYDERGOT  DIHYDROERGOTAMIN DILANTIN  DILAUDID  DILTIAZEM  DIOVAN  DIPHENHYDRAMINE  DIPROLENE  DISULFIRAM  DOCETAXEL  DOFETILIDE  DONEPEZIL  DOVONEX  DOXAZOSIN  DOXORUBICIN  DOXYCYCLINE  DURAGESIC  DUROGESIC  DYAZIDE  DYNACIRC  EBIXA  EFALIZUMAB  EFFEXOR  ELAPRASE  ELIDEL  ELMIRON  EMSAM  ENABLEX  ENALAPRIL  ENBREL  ENOXAPARIN  ENTECAVIR  ENTOCORT  EPLERENONE  EQUASYM  EQUETRO  ERGENYL  ERLOTINIB  ESCITALOPRAM  ETHINYL  ETODOLAC  EUPANTOL  EXCEDRIN  EXELON  EXENATIDE  EXFORGE  EXJADE  EXTENDED  FABRAZYME  FAZACLO  FEIBA  FEMARA  FENTANYL  FERRUM  FLAGYL  FLECAINIDE  FLOMAX  FLONASE  FLOVENT  FLUCONAZOLE  FLUDARABINE  FLUOROURACIL  FLUOXETINE  FLUTICASONE  FOCALIN  FORADIL  FORTEO  FOSAMAX  FOSRENOL  FRAGMIN  FUNGUARD  GABAPENTIN  GABITRIL  GAMMAGARD  GAMUNEX  GAVISCON  GEMZAR  GENOTROPIN  GENTEAL  GEODON  GLEEVEC  GLYCERIN  GLYCOLAX  GOLYTELY  H  HALOPERIDOL  HEPARIN  HEPSERA  HERCEPTIN  HORIZON  HRDROCHLOROTHIAZ HUMIRA  HUMULIN  HYDROCODONE  HYDROMORPHONE  HYDROXYCHLOROQUI HYDROXYUREA  HYPEN  IBUPROFEN  IMATINIB  IMITREX  IMMUNE  IMURAN  INDOCIN  INDOMETHACIN  INFLIXIMAB  INNOHEP  INSULIN  INTRON  INVEGA  IPRATROPIUM  IRINOTECAN  ISONIAZID  ISOSORBIDE  ISOTRETINOIN  ISRADIPINE  ITRIZOLE  KALETRA  KEFLEX  KEPPRA  KINERET  KIOVIG  KIVEXA  LABETALOL  LAMICTAL  LAMISIL  LAMIVUDINE  LAMOTRIGINE  LANSOPRAZOLE  LANTUS  LAPATINIB  LASIX  LEFLUNOMIDE  LEPIRUDIN  LEPONEX  LETAIRIS  LEUPLIN  LEUPLINECTION  LEUPROLIDE  LEVAQUIN  LEVEMIR  LEVOFLOXACIN  LEVOTHYROXINE  LEXAPRO  LIALDA  LIDOCAINE  LIORESAL  LIPITOR  LISDEXAMFETAMINE LISINOPRIL  LISTERINE  LITHIUM  LOCOL  LOPID  LORAZEPAM  LORTAB  LOVAN  LOVASTATIN  LOVAZA  LUCENTIS  LUNESTA  LUPRON  LUVOX  LYRICA  MACUGEN  MAGNESIUM  MALANIL  MANDELAMINE  MARVELON  MAXALT  MEDROXYPROGESTER MELPHALAN  MEMANTINE  MEPRONIZINE  MERCAPTOPURINE  MEROPENEM  METFORMIN  METHADON  METHERGINE  METHOTREXATE  METHYLPHENIDATE  METHYLPREDNISOLO METOCLOPRAMIDE  METOPROLOL  METRONIDAZOLE  MIACALCIN  MIANSERIN  MICARDIS  MIDAZOLAM  MIFEPREX  MIRALAX  MIRAPEX  MIRTAZAPINE  MITOXANTRONE  MONISTAT  MS  MUCOMYST  MYLOTARG  MYOZYME  NAFCILLIN  NAGLAZYME  NALTREXONE  NAMENDA  NANDROLONE  NASALCROM  NASONEX  NATALIZUMAB  NEORAL  NEOSPORIN  NEUPOGEN  NEUPRO  NEURONTIN  NEXIUM  NICOTINE  NIFEDIPINE  NIFLURIL  NIQUITIN  NITRODERM  NORCO  NORDETTE  NORETHINDRONE  NORVASC  NOVANTRONE  NOVATREX  NOVOLOG  NOVOSEVEN  NOXAFIL  NUBAIN  NULYTELY  OLANZAPINE  OLMESARTAN  OMACOR  OMALIZUMAB  OMEPRAZOLE  OMNISCAN  ONICIT  OPTINATE  ORENCIA  ORLISTAT  OROKEN  OTRIVINA  OXACARBEZEPINE  OXCARBAZEPINE  OXYBUTININ  OXYCODONE  PACLITAXEL  PAMIDRONATE  PANALDINE  PANTOLOC  PANTOPRAZOLE  PARACETAMOL  PAROXETINE  PAXIL  PEGETRON  PEMETREXED  PENCICLOVIR  PENTASA  PENTOSTATIN  PERGOLIDE  PERMAX  PHENERGAN  PHENOBARBITAL  PHENOBARBITOL  PHENYTOIN  PHOSBLOCK  PIOGLITAZONE  PIPERACILLIN  PLAQUENIL  PLETAL  POLPER  PRAMIPEXOLE  PRAVASTATIN  PRAZOSIN  PREDNISOLONE  PREDNISONE  PREGABALIN  PREMARIN  PREMPRO  PREVACID  PREZISTA  PRIALT  PRILOSEC  PRIMATENE  PRIMAXIN  PROAIR  PROCRIT  PROGRAF  PROPRANOLOL  PROQUIN  PROTOPIC  PROVENTIL  PROVIGIL  PROZAC  PULMICORT  PYOSTACINE  QUETIAPINE  QUINAPRIL  RABEPRAZOLE  RANEXA  RAPAMUNE  RAPTIVA  REBIF  RECLAST  REGAINE  REGLAN  REMERON  REMICADE  RENAGEL  RENIVACE  REQUIP  RESTASIS  RETEPLASE  REVLIMID  RIBASPHERE  RIBAVIRIN  RIFAMPICIN  RIFAMPIN  RILUTEK  RINDERON  RISEDRONATE  RISPERDAL  RITALIN  ROGAINE  ROSIGLITAZONE  ROZEREM  RYTHMOL  SAIZEN  SALBUTAMOL  SANDOSTATIN  SCOPODER  SEASONALE  SEASONIQUE  SENIOR  SERETIDE  SEROPLEX  SEROPRAM  SEROQUEL  SEROXAT  SERTRALINE  SIFROL  SILVADENE  SIMVASTATIN  SINGULAIR  SIRDALUD  SIROLIMUS  SOMATROPIN  SOMATULINE  SORAFENIB  SORIATANE  SPIRIVA  SPIRONOLACTONE  SPORANOX  SPRYCEL  STADOL  STALEVO  STEDIRIL  STERDEX  STRATTERA  SUBOXONE  SUDAFED  SULFAMETHOXAZOLE SULFATRIM  SULPERAZON  SUTENT  SYMBICORT  SYMLIN  SYNAGIS  TAB  TACLONEX  TACROLIMUS  TAMOXIFEN  TARCEVA  TARGRETIN  TASMAR  TAXOTERE  TAZOCILLINE  TEGRETOL  TEKTURNA  TELMISARTAN  TEMAZEPAM  TEMODAL  TEMOZOLOMIDE  TEMSIROLIMUS  TERBINAFINE  TESTOGEL  THALIDOMIDE  THALOMID  THEOPHYLLINE  THYMOGLOBULIN  THYROID  TIAZAC  TIGECYCLINE  TIOTROPIUM  TIPRANAVIR  TOBRAMYCIN  TOBREX  TOFRANIL  TOPAMAX  TOPROL  TORASEMMEPHA  TORISEL  TRACLEER  TRAMADOL  TRASYLOL  TRELSTAR  TRENTAL  TREVILOR  TRIAMTERENE  TRICOR  TRILEPTAL  TRISENOX  TYGACIL  TYKERB  TYSABRI  ULTRA  UNIRETIC  URSO  URSODEOXYCHOLIC  URSODIOL  VALIUM  VALPROIC  VALTREX  VANCOMYCIN  VAPRISOL  VARENICLINE  VASOTEC  VELCADE  VENLAFAXIINE  VENLAFAXINE  VENTOLIN  VERAMYST  VERAPAMIL  VESICARE  VFEND  VIANITE  VINCRISTINE  VIRAMUNE  VISUDYNE  VIVACTIL  VIVITROL  VOLTAREN  VYTORIN  VYVANSE  WARFARIN  WELCHOL  WELLBUTRIN  WINRHO  XANAX  XELODA  XENICAL  XIGRIS  XOLAIR  XOPENEX  XYREM  XYZAL  ZANTAC  ZAVESCA  ZEFIX  ZELAPAR  ZELDOX  ZELITREX  ZELNORM  ZENAPAX  ZIAGEN  ZIDOVUDINE  ZOCOR  ZOFRAN  ZOLEDRONIC  ZOLOFT  ZOLPIDEM  ZOMETA  ZOMIG  ZONEGRAN  ZONISAMIDE  ZOTON  ZOVIRAX  ZOXAN  ZYBAN  ZYFLO  ZYLET  ZYPREXA  ZYRTEC  ZYVOX  


CONDITION AGGRAVATED : Benadryl Side Effects Report #5483634-5
Consumer or non-health professional from UNITED STATES reported BENADRYL CREAM EXTRA STRENGTH problem on Oct 04, 2007. Female patient, 62 years of age, was diagnosed with dermatitis contact and was treated with BENADRYL CREAM EXTRA STRENGTH. After drug was administered, patient experienced the following problems/side effects: condition aggravated, dermatitis contact, eye swelling, insomnia, lip pain, pruritus, rash erythematous, . BENADRYL CREAM EXTRA STRENGTH dosage: unknown. During the same period patient was treated with BENADRYL CREAM EXTRA STRENGTH, PREDNISONE. Patient recovered.

CONDITION AGGRAVATED : Diovan Side Effects Report #5646648-8
DIOVAN problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2008. Female patient, 85 years of age, was diagnosed with trigeminal neuralgia and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: condition aggravated, trigeminal neuralgia, . DIOVAN dosage: unknown. During the same period patient was treated with NEURONTIN. Patient recovered.

CONDITION AGGRAVATED : Heparin Side Effects Report #5646654-3
Pharmacist from UNITED STATES reported HEPARIN problem on Mar 03, 2008. Male patient, 84 years of age, was diagnosed with thrombosis prophylaxis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: condition aggravated, thrombocytopenia, . HEPARIN dosage: unknown. Patient recovered.

CONDITION AGGRAVATED : Rapamune Side Effects Report #5646686-5
RAPAMUNE problem was reported by a Physician from GERMANY on Feb 27, 2008. Male patient, weighting 143.3 lb, was diagnosed with prophylaxis against transplant rejection and was treated with RAPAMUNE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hepatic enzyme increased, renal failure, . RAPAMUNE dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Enbrel Side Effects Report #5646704-4
Health Professional from SPAIN reported ENBREL problem on Feb 20, 2008. Female patient, 43 years of age, was diagnosed with psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, psoriasis, therapeutic response decreased, . ENBREL dosage: unknown. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Paclitaxel Side Effects Report #5646804-9
PACLITAXEL problem was reported by a Consumer or non-health professional from FRANCE on Feb 25, 2008. Female patient, 78 years of age, was diagnosed with breast cancer metastatic and was treated with PACLITAXEL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, . PACLITAXEL dosage: unknown. During the same period patient was treated with GEMZAR. Patient died on 02/08/2008.

CONDITION AGGRAVATED : Forteo Side Effects Report #5646900-6
Consumer or non-health professional from FRANCE reported FORTEO problem on Feb 25, 2008. Female patient, 77 years of age, was diagnosed with osteoporosis, hypertension and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: condition aggravated, fatigue, foot deformity, thrombophlebitis, . FORTEO dosage: unknown. During the same period patient was treated with PRACTAZIN. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Valtrex Side Effects Report #5646990-0
VALTREX problem was reported by a Physician from JAPAN on Feb 26, 2008. Male patient, 86 years of age, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: condition aggravated, encephalitis, malaise, renal disorder, . VALTREX dosage: 500MG PER DAY. During the same period patient was treated with VICCLOX. Patient was hospitalized. Patient died on 02/12/2008.

CONDITION AGGRAVATED : Proair Side Effects Report #5648339-6
Health Professional from UNITED STATES reported PROAIR HFA problem on Mar 03, 2008. Female patient, 53 years of age, weighting 221.0 lb, was diagnosed with viral upper respiratory tract infection and was treated with PROAIR HFA. After drug was administered, patient experienced the following problems/side effects: condition aggravated, device failure, . PROAIR HFA dosage: unknown. During the same period patient was treated with LEVOXYL. Patient recovered.

CONDITION AGGRAVATED : Mepronizine Side Effects Report #5648499-7
MEPRONIZINE problem was reported by a Consumer or non-health professional from FRANCE on Feb 25, 2008. Male patient, 38 years of age, was treated with MEPRONIZINE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, leukocytosis, myeloproliferative disorder, neutrophilia, . MEPRONIZINE dosage: unknown. During the same period patient was treated with TRANXENE, STILNOX, LEPONEX. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Enbrel Side Effects Report #5648631-5
Physician from JAPAN reported ENBREL problem on Feb 21, 2008. Male patient, weighting 158.7 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, dermatitis psoriasiform, eczema, gastrointestinal perforation, peritonitis, petechiae, . ENBREL dosage: unknown. During the same period patient was treated with OPALMON, AZULFIDINE EN, BUCILLAMINE, FOLIAMIN, PREDONINE, SELBEX. Patient was hospitalized. Patient died on 12/08/2007.

CONDITION AGGRAVATED : Zoloft Side Effects Report #5648945-9
ZOLOFT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 03, 2008. Female patient, weighting 160.0 lb, was diagnosed with depression and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: condition aggravated, depression, diarrhoea, dissociation, feeling abnormal, hyperhidrosis, marital problem, suicide attempt, . ZOLOFT dosage: 150-200MG. 1/DAY PO. During the same period patient was treated with KLONOPIN. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Chantix Side Effects Report #5649488-9
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on Mar 03, 2008. Female patient, 36 years of age, weighting 220.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: condition aggravated, depression, insomnia, suicidal ideation, . CHANTIX dosage: unknown. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Avonex Side Effects Report #5650153-2
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2008. Female patient, 70 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: condition aggravated, coronary artery occlusion, multiple sclerosis, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Xyzal Side Effects Report #5650306-3
Consumer or non-health professional from UNITED STATES reported XYZAL problem on Mar 03, 2008. Female patient, 44 years of age, weighting 135.0 lb, was diagnosed with urticaria and was treated with XYZAL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, dizziness, somnolence, therapeutic response unexpected, urticaria, . XYZAL dosage: 5 MG 1 TIME DAILY PO. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Temozolomide Side Effects Report #5650468-8
TEMOZOLOMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 04, 2008. Male patient, weighting 167.6 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, convulsion, disease progression, glioblastoma, motor dysfunction, sepsis, thrombocytopenia, . TEMOZOLOMIDE dosage: 570 MG. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Tygacil Side Effects Report #5651558-6
Physician from MEXICO reported TYGACIL problem on Feb 11, 2008. Female patient, 52 years of age, was diagnosed with escherichia urinary tract infection, hypertension, diabetes mellitus and was treated with TYGACIL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, multi-organ failure, pancreatitis, . TYGACIL dosage: 100MG INITIAL THEN 50MG EVERY 12 HOURS. During the same period patient was treated with NORVASC, AVAPRO, INSULIN GLARGINE. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Avonex Side Effects Report #5651939-0
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2008. Male patient, 59 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: condition aggravated, epilepsy, . AVONEX dosage: unknown. Patient recovered.

CONDITION AGGRAVATED : Zelnorm Side Effects Report #5652697-6
Physician from UNITED STATES reported ZELNORM problem on Mar 05, 2008. Male patient, weighting 99.00 lb, was diagnosed with mobility decreased and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: condition aggravated, convulsion, influenza, melas syndrome, vomiting, . ZELNORM dosage: 6 MG BID G-TUBE. During the same period patient was treated with LEVETIRACETAM, LORAZEPAM, TIAGABINE, PHENYTOIN, MEMANTINE, THIAMINE, DICHLORACITATE, LANSOPRAZOLE. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Enbrel Side Effects Report #5652920-8
ENBREL problem was reported by a Physician from JAPAN on Feb 22, 2008. Female patient, 74 years of age, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, fungal infection, interstitial lung disease, pneumocystis jiroveci pneumonia, . ENBREL dosage: unknown. During the same period patient was treated with IMURAN, PREDONINE. Patient was hospitalized. Patient died on 11/26/2006.

CONDITION AGGRAVATED : Avonex Side Effects Report #5654377-X
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Feb 20, 2008. Female patient, 57 years of age, weighting 115.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: condition aggravated, delusion, kidney infection, multiple sclerosis, urinary tract infection, weight decreased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Paclitaxel Side Effects Report #5655301-6
PACLITAXEL problem was reported by a Consumer or non-health professional from FRANCE on Feb 29, 2008. Female patient, 79 years of age, was diagnosed with breast cancer metastatic and was treated with PACLITAXEL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, . PACLITAXEL dosage: unknown. During the same period patient was treated with GEMZAR. Patient died on 02/08/2008.

CONDITION AGGRAVATED : Azulfidine Side Effects Report #5655993-1
Consumer or non-health professional from JAPAN reported AZULFIDINE EN problem on Feb 26, 2008. Male patient, weighting 158.7 lb, was diagnosed with rheumatoid arthritis and was treated with AZULFIDINE EN. After drug was administered, patient experienced the following problems/side effects: condition aggravated, eczema, gastrointestinal perforation, petechiae, . AZULFIDINE EN dosage: unknown. During the same period patient was treated with ETANERCEPT, LIMAPROST, FOLIAMIN, PREDNISOLONE, TEPRENONE, ETODOLAC, PYRIDOXAL PHOSPHATE, BUCILLAMINE. Patient was hospitalized. Patient died on 12/08/2007.

CONDITION AGGRAVATED : Effexor Side Effects Report #5656679-X
EFFEXOR problem was reported by a Health Professional from NETHERLANDS on Mar 05, 2008. Female patient was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: condition aggravated, disturbance in attention, emotional disorder, multiple sclerosis, . EFFEXOR dosage: unknown. Patient recovered.

CONDITION AGGRAVATED : Lexapro Side Effects Report #5656766-6
Consumer or non-health professional from UNITED STATES reported LEXAPRO problem on Mar 07, 2008. Female patient, 27 years of age, weighting 130.0 lb, was diagnosed with anxiety, depression and was treated with LEXAPRO. After drug was administered, patient experienced the following problems/side effects: condition aggravated, depression, suicide attempt, . LEXAPRO dosage: unknown. During the same period patient was treated with CELEXA. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Chantix Side Effects Report #5657494-3
CHANTIX problem was reported by a Pharmacist from UNITED STATES on Mar 07, 2008. Male patient, 51 years of age, weighting 188.3 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: condition aggravated, convulsion, . CHANTIX dosage: STARTER PACK AS DIRECEDTED PO 1MG TABLETS BID PO. Patient recovered.

CONDITION AGGRAVATED : Avonex Side Effects Report #5659361-8
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Feb 22, 2008. Female patient, 53 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: condition aggravated, malaise, multiple sclerosis, . AVONEX dosage: unknown. Patient died on 02/10/2008.

CONDITION AGGRAVATED : Phenobarbitol Side Effects Report #5659515-0
PHENOBARBITOL problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 07, 2008. Female patient, 17 years of age, weighting 110.0 lb, was diagnosed with convulsion and was treated with PHENOBARBITOL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, convulsion, . PHENOBARBITOL dosage: unknown. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Prednisolone Side Effects Report #5660166-2
Consumer or non-health professional from UNITED STATES reported PREDNISOLONE problem on Mar 10, 2008. Female patient, child 6 years of age, weighting 66.00 lb, was diagnosed with rash and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, monoplegia, pain in extremity, pruritus, rash, sensory loss, . PREDNISOLONE dosage: unknown. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Enbrel Side Effects Report #5660341-7
ENBREL problem was reported by a Physician from JAPAN on Feb 27, 2008. Female patient, weighting 149.9 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, interstitial lung disease, pancreatitis acute, . ENBREL dosage: unknown. During the same period patient was treated with MEDROL, NEOISCOTIN, AMLODIN, LANSOPRAZOLE, VOLTAREN, PYRIDOXAL PHOSPHATE, ZOLPIDEM TARTRATE, HOKUNALIN. Patient was hospitalized. Patient died on 11/19/2007.

CONDITION AGGRAVATED : Gaviscon Side Effects Report #5660876-7
Health Professional from FRANCE reported GAVISCON problem on Feb 29, 2008. Male patient was treated with GAVISCON. After drug was administered, patient experienced the following problems/side effects: condition aggravated, cytolytic hepatitis, serum ferritin increased, transferrin saturation decreased, . GAVISCON dosage: unknown. During the same period patient was treated with EQUANIL, VALIUM, AOTAL, STILNOX, OMEPRAZOLE. Patient recovered.

CONDITION AGGRAVATED : Diovan Side Effects Report #5661530-8
DIOVAN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 05, 2008. Female patient, 85 years of age, was diagnosed with trigeminal neuralgia and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: condition aggravated, trigeminal neuralgia, . DIOVAN dosage: unknown. During the same period patient was treated with NEURONTIN. Patient recovered.

CONDITION AGGRAVATED : Tacrolimus Side Effects Report #5661621-1
Physician from JAPAN reported TACROLIMUS CAPSULES problem on Feb 19, 2008. Female patient, 69 years of age, weighting 100.3 lb, was diagnosed with rheumatoid arthritis and was treated with TACROLIMUS CAPSULES. After drug was administered, patient experienced the following problems/side effects: condition aggravated, interstitial lung disease, . TACROLIMUS CAPSULES dosage: unknown. During the same period patient was treated with PREDNISOLONE, SOL MEDROL, METHYCOBAL, DEPAS, MUCOSTA, MEXITIL, MAGNESIUM OXIDE, JUVELA. Patient died on 07/01/2007.

CONDITION AGGRAVATED : Femara Side Effects Report #5662170-7
FEMARA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 10, 2008. Female patient, weighting 282.6 lb, was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: condition aggravated, psoriasis, . FEMARA dosage: 2.5 MG. Patient recovered.

CONDITION AGGRAVATED : Enbrel Side Effects Report #5662756-X
Physician from COLOMBIA reported ENBREL problem on Feb 28, 2008. Male patient, 42 years of age, weighting 158.7 lb, was diagnosed with psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, osteonecrosis, psoriasis, . ENBREL dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

CONDITION AGGRAVATED : Citalopram Side Effects Report #5662801-1
CITALOPRAM HYDROBROMIDE problem was reported by a Pharmacist from UNITED STATES on Mar 11, 2008. Female patient, 39 years of age, was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, dysphemia, feeling cold, muscle disorder, muscle rigidity, tremor, . CITALOPRAM HYDROBROMIDE dosage: unknown. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Letairis Side Effects Report #5663205-8
Pharmacist from UNITED STATES reported LETAIRIS problem on Mar 11, 2008. Male patient was diagnosed with pulmonary hypertension and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: condition aggravated, dyspnoea, pain in extremity, . LETAIRIS dosage: 5MG DAILY PO. Patient recovered.

CONDITION AGGRAVATED : Restasis Side Effects Report #5663212-5
RESTASIS problem was reported by a Health Professional from UNITED STATES on Mar 11, 2008. Female patient, 63 years of age, weighting 145.0 lb, was diagnosed with dry eye and was treated with RESTASIS. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hypertension, instillation site irritation, . RESTASIS dosage: unknown. Patient recovered.

CONDITION AGGRAVATED : Lamisil Side Effects Report #5663605-6
Consumer or non-health professional from GERMANY reported LAMISIL problem on Feb 20, 2008. Male patient, 72 years of age, weighting 160.9 lb, was diagnosed with tinea pedis and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: condition aggravated, crying, open wound, pain, skin haemorrhage, skin inflammation, wound secretion, . LAMISIL dosage: unknown. During the same period patient was treated with BATRAFEN, CHINOSOL, IMAZOL PASTE, EPIPEVISONE. Patient recovered.

CONDITION AGGRAVATED : Naglazyme Side Effects Report #5663681-0
NAGLAZYME problem was reported by a Physician from BRAZIL on Feb 22, 2008. Male patient, child 7 years of age, weighting 32.19 lb, was diagnosed with mucopolysaccharidosis vi and was treated with NAGLAZYME. After drug was administered, patient experienced the following problems/side effects: condition aggravated, diffuse axonal injury, gait disturbance, hypotonia, intervertebral disc disorder, muscle spasticity, oxygen saturation decreased, pyramidal tract syndrome, . NAGLAZYME dosage: 1.5 ML;QM;INTH;15 MG;X1;IV. Patient recovered.

CONDITION AGGRAVATED : Fluticasone Side Effects Report #5663710-4
Consumer or non-health professional from UNITED STATES reported FLUTICASONE PROPIONATE problem on Mar 03, 2008. Female patient was treated with FLUTICASONE PROPIONATE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, cushing's syndrome, kaposi's sarcoma, . FLUTICASONE PROPIONATE dosage: unknown. Patient recovered.

CONDITION AGGRAVATED : Urso Side Effects Report #5663845-6
URSO problem was reported by a Consumer or non-health professional from JAPAN on Mar 04, 2008. Female patient, 55 years of age, was diagnosed with hepatic function abnormal, rheumatoid arthritis and was treated with URSO. After drug was administered, patient experienced the following problems/side effects: condition aggravated, erythema, rheumatoid arthritis, vasculitis necrotising, . URSO dosage: 300 MG/DAY ORAL. During the same period patient was treated with REMICADE, RHEUMATREX, FOLIC ACID, ACTONEL, PREDNISOLONE. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Novantrone Side Effects Report #5664140-1
Consumer or non-health professional from UNITED STATES reported NOVANTRONE problem on Feb 27, 2008. Male patient, 28 years of age, was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, diverticulitis, white blood cell count decreased, . NOVANTRONE dosage: unknown. During the same period patient was treated with COPAXONE. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Rebif Side Effects Report #5664157-7
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 26, 2008. Male patient, 48 years of age, weighting 140.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: condition aggravated, hepatic enzyme increased, trigeminal neuralgia, . REBIF dosage: unknown. During the same period patient was treated with ATENOLOL, BACLOFEN, EFFEXOR. Patient recovered.

CONDITION AGGRAVATED : Rebif Side Effects Report #5664167-X
Consumer or non-health professional from UNITED STATES reported REBIF problem on Feb 27, 2008. Female patient, 56 years of age, weighting 148.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: condition aggravated, constipation, cystitis, decreased appetite, diarrhoea, injection site reaction, irritability, urinary incontinence, urinary retention, . REBIF dosage: unknown. Patient recovered.

CONDITION AGGRAVATED : Avonex Side Effects Report #5664178-4
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 29, 2008. Female patient, 58 years of age, weighting 145.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: condition aggravated, exostosis, fall, multiple sclerosis, pain, rotator cuff syndrome, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

CONDITION AGGRAVATED : Avonex Side Effects Report #5664180-2
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Mar 04, 2008. Male patient, 44 years of age, weighting 180.0 l