CUSHING'S SYNDROME side effect
What is CUSHING'S SYNDROME ?Drugs associated with CUSHING'S SYNDROME
ADVAIR AREDIA BICALUTAMIDE BYETTA CELLCEPT CLOBETASOL COMBIVIR DECADRON ENBREL FLOVENT FLUTICASONE GLEEVEC HYDROQUINONE KENALOG KEPPRA LEUPROLIDE NIFEDIPINE PREDNISONE REBIF REMICADE SERETIDE SPORANOX TEMOZOLOMIDE VALTREX VIANI XENICAL ZYPREXACUSHING'S SYNDROME : Zyprexa Side Effects Report #5622836-1
Consumer or non-health professional from FRANCE reported ZYPREXA problem on Feb 05, 2008. Female patient was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . ZYPREXA dosage: unknown. Patient recovered.
CUSHING'S SYNDROME : Kenalog Side Effects Report #5637226-5
KENALOG problem was reported by a Physician from UNITED STATES on July 18, 2007. Female patient, 20 years of age, was diagnosed with prophylaxis and was treated with KENALOG. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, pruritus, . KENALOG dosage: unknown. During the same period patient was treated with VICODIN. Patient recovered.
CUSHING'S SYNDROME : Aredia Side Effects Report #5604122-9
Consumer or non-health professional from ITALY reported AREDIA problem on Jan 21, 2008. Female patient was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, mastication disorder, osteonecrosis, surgery, . AREDIA dosage: unknown. During the same period patient was treated with ZOMETA. Patient died on 12/25/2004.
CUSHING'S SYNDROME : Rebif Side Effects Report #5604860-8
REBIF problem was reported by a Physician from UNITED STATES on Jan 11, 2008. Female patient, 36 years of age, weighting 230.0 lb, was diagnosed with multiple sclerosis, multiple sclerosis relapse and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, influenza like illness, injection site reaction, multiple sclerosis relapse, myalgia, pain, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Leuprolide Side Effects Report #5565867-2
Physician from AUSTRIA reported LEUPROLIDE ACETATE problem on Dec 10, 2007. Male patient, 70 years of age, was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . LEUPROLIDE ACETATE dosage: 11.25 MG (11.25 MG, 1 IN 3 M). Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Leuprolide Side Effects Report #5569743-0
LEUPROLIDE ACETATE problem was reported by a Consumer or non-health professional from AUSTRIA on Dec 14, 2007. Male patient, 73 years of age, was diagnosed with neoplasm prostate and was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, paraneoplastic syndrome, . LEUPROLIDE ACETATE dosage: 11.25 MG (11.25 MG, 1 IN 3 M) SUBCUTANEOUS. During the same period patient was treated with BISOPROLOL, MARCUMAR, DEFLAMAT, ZOMETA. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Keppra Side Effects Report #5573650-7
Physician from UNITED STATES reported KEPPRA problem on Dec 03, 2007. Female patient, 59 years of age, weighting 194.0 lb, was diagnosed with glioblastoma multiforme and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, glioblastoma multiforme, lymphopenia, malignant neoplasm progression, opportunistic infection, oral candidiasis, . KEPPRA dosage: 500 MG 2/D PO. During the same period patient was treated with TEMOZOLOMIDE, BACTRIM DS, DECADRON. Patient was hospitalized. Patient died on 11/23/2007.
CUSHING'S SYNDROME : Sporanox Side Effects Report #5576731-7
SPORANOX problem was reported by a Physician from KOREA, REPUBLIC OF on Dec 20, 2007. Female patient was diagnosed with tinea pedis, onychomycosis, keloid scar and was treated with SPORANOX. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . SPORANOX dosage: unknown. During the same period patient was treated with TRIAMCINOLONE, LIDOCAINE. Patient recovered.
CUSHING'S SYNDROME : Temozolomide Side Effects Report #5514826-4
Physician from UNITED STATES reported TEMOZOLOMIDE problem on Nov 05, 2007. Female patient, 59 years of age, weighting 194.0 lb, was diagnosed with glioblastoma multiforme and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, glioblastoma multiforme, lymphopenia, malignant neoplasm progression, opportunistic infection, oral candidiasis, . TEMOZOLOMIDE dosage: 75 MG/M2;QD;PO ; 1450 MG; PO. During the same period patient was treated with BACTRIM DS, DECADRON, KEPPRA. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Temozolomide Side Effects Report #5527445-0
TEMOZOLOMIDE problem was reported by a Physician from UNITED STATES on Nov 19, 2007. Female patient, 59 years of age, weighting 194.0 lb, was diagnosed with glioblastoma multiforme and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, glioblastoma multiforme, lymphopenia, malignant neoplasm progression, oral candidiasis, . TEMOZOLOMIDE dosage: 75 MG/M2; QD; PO; 1450 MG; PO. During the same period patient was treated with BACTRIM DS, DECADRON, KEPPRA. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Fluticasone Side Effects Report #5531277-7
Health Professional from CANADA reported FLUTICASONE PROPIONATE problem on Nov 12, 2007. Female patient, 43 years of age, was diagnosed with hiv infection and was treated with FLUTICASONE PROPIONATE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, nausea, . FLUTICASONE PROPIONATE dosage: unknown. During the same period patient was treated with LOPINAVIR AND RITONAVIR, ABACAVIR SULPHATE, DIDANOSINE. Patient recovered.
CUSHING'S SYNDROME : Valtrex Side Effects Report #5475793-5
VALTREX problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 27, 2007. Female patient, 18 years of age, was diagnosed with genital herpes, pruritus and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, cushingoid, hirsutism, ill-defined disorder, . VALTREX dosage: 500MG TWICE PER DAY. During the same period patient was treated with WESTCORT, CLOBETASOL PROPIONATE, VISTARIL, XYLOCAINE. Patient recovered.
CUSHING'S SYNDROME : Flovent Side Effects Report #5486761-1
Consumer or non-health professional from UNITED STATES reported FLOVENT problem on Oct 15, 2007. Female patient, child 1 years of age, was diagnosed with asthma and was treated with FLOVENT. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . FLOVENT dosage: unknown. During the same period patient was treated with ATIVAN, LEVOTHYROXINE, POTASSIUM CHLORIDE, PREVACID, ALBUTEROL, CALCIUM CARBONATE, FOLATE, BUMEX. Patient recovered.
CUSHING'S SYNDROME : Advair Side Effects Report #5497352-0
ADVAIR DISKUS problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 06, 2006. Female patient was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . ADVAIR DISKUS dosage: unknown. Patient recovered.
CUSHING'S SYNDROME : Advair Side Effects Report #5497584-1
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on Dec 12, 2006. Male patient was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . ADVAIR DISKUS dosage: unknown. Patient recovered.
CUSHING'S SYNDROME : Combivir Side Effects Report #5448736-8
COMBIVIR problem was reported by a Physician from AUSTRALIA on Sept 04, 2007. Female patient was treated with COMBIVIR. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . COMBIVIR dosage: unknown. During the same period patient was treated with KALETRA. Patient recovered.
CUSHING'S SYNDROME : Valtrex Side Effects Report #5453828-3
Consumer or non-health professional from UNITED STATES reported VALTREX problem on Sept 11, 2007. Female patient, 18 years of age, was diagnosed with genital herpes, pruritus and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, cushingoid, hirsutism, ill-defined disorder, . VALTREX dosage: 500MG TWICE PER DAY. During the same period patient was treated with WESTCORT, VISTARIL. Patient recovered.
CUSHING'S SYNDROME : Gleevec Side Effects Report #5470549-1
GLEEVEC problem was reported by a Consumer or non-health professional from FRANCE on Sept 26, 2007. Female patient, 49 years of age, was diagnosed with chronic myeloid leukaemia and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, muscle spasms, . GLEEVEC dosage: 400 MG, QD. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Remicade Side Effects Report #5376759-6
Health Professional from UNITED STATES reported REMICADE problem on June 21, 2007. Female patient, weighting 265.0 lb, was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, diarrhoea, . REMICADE dosage: unknown. Patient recovered.
CUSHING'S SYNDROME : Xenical Side Effects Report #5389377-0
XENICAL problem was reported by a Consumer or non-health professional from UNITED KINGDOM on July 05, 2007. Female patient, 26 years of age, weighting 254.9 lb, was diagnosed with obesity and was treated with XENICAL. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . XENICAL dosage: unknown. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Bicalutamide Side Effects Report #5397934-0
Health Professional from JAPAN reported BICALUTAMIDE problem on July 19, 2007. Male patient, 78 years of age, was treated with BICALUTAMIDE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . BICALUTAMIDE dosage: unknown. During the same period patient was treated with LEUPROLIDE ACETATE. Patient recovered.
CUSHING'S SYNDROME : Remicade Side Effects Report #5376759-6
REMICADE problem was reported by a Health Professional from UNITED STATES on June 21, 2007. Female patient, weighting 265.0 lb, was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, diarrhoea, . REMICADE dosage: unknown. Patient recovered.
CUSHING'S SYNDROME : Xenical Side Effects Report #5389377-0
Consumer or non-health professional from UNITED KINGDOM reported XENICAL problem on July 05, 2007. Female patient, 26 years of age, weighting 254.9 lb, was diagnosed with obesity and was treated with XENICAL. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . XENICAL dosage: unknown. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Bicalutamide Side Effects Report #5397934-0
BICALUTAMIDE problem was reported by a Health Professional from JAPAN on July 19, 2007. Male patient, 78 years of age, was treated with BICALUTAMIDE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . BICALUTAMIDE dosage: unknown. During the same period patient was treated with LEUPROLIDE ACETATE. Patient recovered.
CUSHING'S SYNDROME : 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.
CUSHING'S SYNDROME : Nifedipine Side Effects Report #5670282-7
NIFEDIPINE problem was reported by a Consumer or non-health professional from JAPAN on Mar 12, 2008. Female patient, 32 years of age, was diagnosed with hypertension and was treated with NIFEDIPINE. After drug was administered, patient experienced the following problems/side effects: adrenal adenoma, cushing's syndrome, foetal growth retardation, pregnancy, . NIFEDIPINE dosage: unknown. During the same period patient was treated with METHYLDOPA. Patient recovered.
CUSHING'S SYNDROME : Enbrel Side Effects Report #5621683-4
Physician from UNITED STATES reported ENBREL problem on Jan 28, 2008. Female patient, weighting 187.2 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: conjunctivitis, cushing's syndrome, depression, glomerulonephritis minimal lesion, hiatus hernia, lymphadenopathy, myalgia, nephrotic syndrome, oedema peripheral, . ENBREL dosage: unknown. During the same period patient was treated with DOXYLAMINE SUCCINATE, SYNTHROID, CALCIUM GLUCONATE, VITAMIN B, ADVAIR DISKUS, FOSAMAX, VITAMIN D. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Clobetasol Side Effects Report #5625260-0
CLOBETASOL PROPIONATE problem was reported by a Consumer or non-health professional from TURKEY on Jan 07, 2008. Female patient was diagnosed with dermatitis diaper and was treated with CLOBETASOL PROPIONATE. After drug was administered, patient experienced the following problems/side effects: aspartate aminotransferase increased, cushing's syndrome, escherichia urinary tract infection, platelet count increased, . CLOBETASOL PROPIONATE dosage: unknown. Patient recovered.
CUSHING'S SYNDROME : Kenalog Side Effects Report #5637245-9
Consumer or non-health professional from UNITED STATES reported KENALOG problem on June 01, 2007. Male patient, 26 years of age, weighting 260.1 lb, was diagnosed with back pain and was treated with KENALOG. After drug was administered, patient experienced the following problems/side effects: adrenal insufficiency, cushing's syndrome, hypertension, . KENALOG dosage: unknown. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Byetta Side Effects Report #5653944-7
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 05, 2007. Female patient, 58 years of age, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: contusion, cushing's syndrome, decreased appetite, injection site haemorrhage, . BYETTA dosage: unknown. Patient recovered.
CUSHING'S SYNDROME : Cellcept Side Effects Report #5574623-0
Physician from GERMANY reported CELLCEPT problem on Dec 14, 2007. Female patient, 69 years of age, weighting 154.3 lb, was diagnosed with vasculitis, pain, pulmonary embolism and was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: angina pectoris, cushing's syndrome, hepatitis, hereditary haemochromatosis, hypertensive cardiomegaly, nerve root lesion, osteonecrosis, pancreatitis, paresis, . CELLCEPT dosage: REPORTED: 3 X 500 MG.. During the same period patient was treated with CIPRO, TARGIN, MARCUMAR, NOVALGIN, FOSAMAX, PASPERTIN, CYMBALTA, DIFLUCAN. Patient recovered.
CUSHING'S SYNDROME : Hydroquinone Side Effects Report #5506174-3
HYDROQUINONE problem was reported by a Physician from BELGIUM on Oct 18, 2007. Female patient, 24 years of age, was treated with HYDROQUINONE. After drug was administered, patient experienced the following problems/side effects: amenorrhoea, cushing's syndrome, hypertension, skin ulcer, . HYDROQUINONE dosage: unknown. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Clobetasol Side Effects Report #5506198-6
Physician from BELGIUM reported CLOBETASOL problem on Oct 18, 2007. Female patient, 24 years of age, was treated with CLOBETASOL. After drug was administered, patient experienced the following problems/side effects: amenorrhoea, cushing's syndrome, hypertension, iatrogenic injury, skin ulcer, . CLOBETASOL dosage: unknown. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Decadron Side Effects Report #5509342-X
DECADRON problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 31, 2007. Female patient, 59 years of age, weighting 194.0 lb, was diagnosed with glioblastoma multiforme and was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: asthenia, cushing's syndrome, disease progression, lymphopenia, systemic candida, . DECADRON dosage: 4 MG/DAILY/PO. During the same period patient was treated with TEMODAR, BACTRIM DS, KEPPRA, PRILOSEC, SYNTHROID, VALTREX, FLUCONAZOLE. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Keppra Side Effects Report #5520543-7
Physician from UNITED STATES reported KEPPRA problem on Oct 29, 2007. Female patient, 59 years of age, weighting 194.0 lb, was diagnosed with glioblastoma multiforme and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: asthenia, cushing's syndrome, glioblastoma multiforme, lymphopenia, malignant neoplasm progression, systemic candida, . KEPPRA dosage: 500 MG 2/D PO. During the same period patient was treated with TEMOZOLOMIDE, BACTRIM DS, DECADRON. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Decadron Side Effects Report #5523053-6
DECADRON UNK problem was reported by a Health Professional from UNITED STATES on Nov 14, 2007. Female patient, 59 years of age, weighting 194.0 lb, was diagnosed with glioblastoma multiforme and was treated with DECADRON UNK. After drug was administered, patient experienced the following problems/side effects: asthenia, cushing's syndrome, glioblastoma multiforme, malignant neoplasm progression, oral candidiasis, . DECADRON UNK dosage: 4 MG DAILY PO. During the same period patient was treated with TEMODAR, BACTRIM DS, KEPPRA, PRILOSEC, SYNTHROID, VALTREX. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Fluticasone Side Effects Report #5531278-9
Consumer or non-health professional from CANADA reported FLUTICASONE PROPIONATE problem on Nov 12, 2007. Female patient, 37 years of age, was diagnosed with hiv infection and was treated with FLUTICASONE PROPIONATE. After drug was administered, patient experienced the following problems/side effects: acne, cushing's syndrome, skin striae, . FLUTICASONE PROPIONATE dosage: unknown. During the same period patient was treated with LOPINAVIR AND RITONAVIR, COMBIVIR. Patient recovered.
CUSHING'S SYNDROME : Temozolomide Side Effects Report #5532369-9
TEMOZOLOMIDE problem was reported by a Physician from UNITED STATES on Nov 20, 2007. Female patient, 59 years of age, weighting 194.0 lb, was diagnosed with glioblastoma multiforme and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, cushing's syndrome, glioblastoma multiforme, lymphopenia, malignant neoplasm progression, oral candidiasis, . TEMOZOLOMIDE dosage: 75 MG/M2;QD;PO ; 1450 MG;PO. During the same period patient was treated with BACTRIM DS, DECADRON, KEPPRA. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Clobetasol Side Effects Report #5478857-5
Physician from TURKEY reported CLOBETASOL PROPIONATE problem on Aug 31, 2007. Female patient, 48 years of age, was diagnosed with eczema and was treated with CLOBETASOL PROPIONATE. After drug was administered, patient experienced the following problems/side effects: condition aggravated, cushing's syndrome, skin candida, . CLOBETASOL PROPIONATE dosage: unknown. Patient recovered.
CUSHING'S SYNDROME : Prednisone Side Effects Report #5449136-7
PREDNISONE problem was reported by a Consumer or non-health professional from on Sept 06, 2007. Female patient was diagnosed with pulmonary sarcoidosis, granulomatous liver disease and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: cardio-respiratory arrest, cushing's syndrome, . PREDNISONE dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, FUROSEMIDE. Patient died on 08/04/2005.
CUSHING'S SYNDROME : Seretide Side Effects Report #5399255-9
Physician from FRANCE reported SERETIDE DISKUS problem on July 19, 2007. Female patient, 40 years of age, weighting 112.4 lb, was diagnosed with asthma, hiv infection and was treated with SERETIDE DISKUS. After drug was administered, patient experienced the following problems/side effects: blood cortisol decreased, cushing's syndrome, skin striae, weight increased, . SERETIDE DISKUS dosage: unknown. During the same period patient was treated with NORVIR, TELZIR, TRUVADA. Patient recovered.
CUSHING'S SYNDROME : Seretide Side Effects Report #5400362-2
SERETIDE DISKUS problem was reported by a Physician from FRANCE on July 19, 2007. Female patient, 40 years of age, weighting 112.4 lb, was diagnosed with asthma, hiv infection and was treated with SERETIDE DISKUS. After drug was administered, patient experienced the following problems/side effects: blood cortisol decreased, cushing's syndrome, skin striae, weight increased, . SERETIDE DISKUS dosage: unknown. During the same period patient was treated with NORVIR, TELZIR, TRUVADA. Patient recovered.
CUSHING'S SYNDROME : Seretide Side Effects Report #5399255-9
Physician from FRANCE reported SERETIDE DISKUS problem on July 19, 2007. Female patient, 40 years of age, weighting 112.4 lb, was diagnosed with asthma, hiv infection and was treated with SERETIDE DISKUS. After drug was administered, patient experienced the following problems/side effects: blood cortisol decreased, cushing's syndrome, skin striae, weight increased, . SERETIDE DISKUS dosage: unknown. During the same period patient was treated with NORVIR, TELZIR, TRUVADA. Patient recovered.
CUSHING'S SYNDROME : Seretide Side Effects Report #5400362-2
SERETIDE DISKUS problem was reported by a Physician from FRANCE on July 19, 2007. Female patient, 40 years of age, weighting 112.4 lb, was diagnosed with asthma, hiv infection and was treated with SERETIDE DISKUS. After drug was administered, patient experienced the following problems/side effects: blood cortisol decreased, cushing's syndrome, skin striae, weight increased, . SERETIDE DISKUS dosage: unknown. During the same period patient was treated with NORVIR, TELZIR, TRUVADA. Patient recovered.
CUSHING'S SYNDROME : Fluticasone Side Effects Report #5672433-7
Physician from UNITED STATES reported FLUTICASONE PROPIONATE problem on Mar 06, 2008. Male patient, 60 years of age, was diagnosed with asthma and was treated with FLUTICASONE PROPIONATE. After drug was administered, patient experienced the following problems/side effects: adrenal suppression, condition aggravated, cushing's syndrome, fatigue, hiv wasting syndrome, hypertension, iatrogenic injury, kaposi's sarcoma, . FLUTICASONE PROPIONATE dosage: unknown. During the same period patient was treated with ATAZANAVIR SULPHATE, DIDANOSINE, TENOFOVIR, LOPINAVIR AND RITONAVIR, EMTRICITABINE, GROWTH HORMONE, NANDROLONE DECANOATE. Patient recovered.
CUSHING'S SYNDROME : Viani Side Effects Report #5608007-3
VIANI problem was reported by a Consumer or non-health professional from GERMANY on Jan 28, 2008. Female patient, 21 years of age, was treated with VIANI. After drug was administered, patient experienced the following problems/side effects: blood count abnormal, central obesity, cushing's syndrome, depression, erythema, oedema, skin striae, . VIANI dosage: unknown. During the same period patient was treated with CORTISONE, VIANI MITE. Patient recovered.
CUSHING'S SYNDROME : Temozolomide Side Effects Report #5509756-8
Consumer or non-health professional from UNITED STATES reported TEMOZOLOMIDE problem on Nov 07, 2007. Female patient, weighting 194.0 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: asthenia, candidiasis, cushing's syndrome, disease progression, glioblastoma multiforme, lymphopenia, . TEMOZOLOMIDE dosage: 1450 MG. During the same period patient was treated with BACTRIM DS, DECADRON, KEPPRA. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Temozolomide Side Effects Report #5530432-X
TEMOZOLOMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 27, 2007. Female patient, weighting 194.0 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: asthenia, candidiasis, cushing's syndrome, glioblastoma multiforme, lymphopenia, malignant neoplasm progression, . TEMOZOLOMIDE dosage: 1450 MG. During the same period patient was treated with BACTRIM DS, DECADRON, KEPPRA. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Keppra Side Effects Report #5533991-6
Physician from UNITED STATES reported KEPPRA problem on Nov 15, 2007. Female patient, 59 years of age, weighting 194.0 lb, was diagnosed with glioblastoma multiforme and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, asthenia, cushing's syndrome, glioblastoma multiforme, lymphopenia, malignant neoplasm progression, opportunistic infection, oral candidiasis, . KEPPRA dosage: 500 MG 2/D PO. During the same period patient was treated with TEMOZOLOMIDE, BACTRIM DS, DECADRON. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Temozolomide Side Effects Report #5493114-9
TEMOZOLOMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 22, 2007. Female patient, weighting 194.0 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: asthenia, candidiasis, cushing's syndrome, glioblastoma multiforme, neoplasm recurrence, . TEMOZOLOMIDE dosage: 1450 MG. During the same period patient was treated with BACTRIM DS, DECADRON, KEPPRA. Patient was hospitalized. Patient recovered.
CUSHING'S SYNDROME : Temozolomide Side Effects Report #5501311-9
Physician from UNITED STATES reported TEMOZOLOMIDE problem on Oct 19, 2007. Female patient, 59 years of age, weighting 194.0 lb, was diagnosed with glioblastoma multiforme and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: asthenia, candidiasis, cushing's syndrome, glioblastoma multiforme, lymphopenia, malignant neoplasm progression, . TEMOZOLOMIDE dosage: 75 MG/M2;QD;PO. During the same period patient was treated with BACTRIM DS, DECADRON, KEPPRA. Patient was hospitalized. Patient recovered.