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CUSHING'S SYNDROME side effect

What is CUSHING'S SYNDROME ?
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Drugs associated with CUSHING'S SYNDROME

ADVAIR  ALVESCO  AOTAL  ASMANEX  BICALUTAMIDE  BYETTA  CELLCEPT  CLOBETASOL  DAIVOBET  DECADRON  ENBREL  ETONORGESTREL  FLOVENT  FLUTICASONE  GLEEVEC  HYDROCORTONE  HYDROQUINONE  KENALOG  KEPPRA  LEUPROLIDE  LOPINAVIR  NIFEDIPINE  PREDNISOLONE  PULMICORT  REBIF  REMICADE  RITONAVIR  SERETIDE  SEROQUEL  SPORANOX  SYMBICORT  TEMODAL  TEMOZOLOMIDE  VALTREX  VIANI  XENICAL  


Kenalog Side Effects Report #5637226-5
Physician from UNITED STATES reported KENALOG problem 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.

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.

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.

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.


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.

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.

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.

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.

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.


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.

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.

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.

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.

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.


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.

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.

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.

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.

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.


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.

Remicade Side Effects Report #5738968-3
Consumer or non-health professional from UNITED STATES reported REMICADE problem on May 08, 2008. Female patient, weighting 190.0 lb, was diagnosed with colitis ulcerative and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, intervertebral disc protrusion, . REMICADE dosage: unknown. Patient recovered.

Etonorgestrel Side Effects Report #5753950-8
ETONORGESTREL problem was reported by a Health Professional from CHILE on May 14, 2008. Female patient, 21 years of age, was diagnosed with contraception and was treated with ETONORGESTREL. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, depression, iatrogenic injury, skin striae, vogt-koyanagi-harada syndrome, . ETONORGESTREL dosage: unknown. Patient recovered.

Ritonavir Side Effects Report #5696440-3
Consumer or non-health professional from UNITED STATES reported RITONAVIR problem on Mar 27, 2008. Male patient, 60 years of age, was diagnosed with hiv infection, asthma and was treated with RITONAVIR. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, kaposi's sarcoma aids related, . RITONAVIR dosage: unknown. During the same period patient was treated with LOPINAVIR AND RITONAVIR, FLUTICASONE, ATAZANAVIR SULPHATE, DIDANOSINE, TENOFOVIR, EMTRICITABINE, SALMETEROL. Patient recovered.

Clobetasol Side Effects Report #5705264-X
CLOBETASOL PROPIONATE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 27, 2008. Female patient, 28 years of age, was diagnosed with skin discolouration and was treated with CLOBETASOL PROPIONATE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, genital candidiasis, infertility female, myopathy, . CLOBETASOL PROPIONATE dosage: unknown. Patient recovered.

Alvesco Side Effects Report #5724566-4
Consumer or non-health professional from SWITZERLAND reported ALVESCO problem on Sept 28, 2007. Male patient, 60 years of age, was diagnosed with asthma and was treated with ALVESCO. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . ALVESCO dosage: unknown. During the same period patient was treated with ITRACONAZOLE, PREDNISONE, CALCIUM CARBONATE COLECALCIFEROL, ESOMEPRAZOLE, NITRAZEPAM, AMBROXIL HYDROCHLORIDE. Patient recovered.

Lopinavir Side Effects Report #5357794-0
LOPINAVIR problem was reported by a Consumer or non-health professional from UNITED STATES on June 05, 2007. Male patient, child 9 years of age, weighting 53.57 lb, was diagnosed with hiv infection cdc category a1, asthma, rhinitis allergic and was treated with LOPINAVIR. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . LOPINAVIR dosage: 216/54 MG (230/57.5 MG/M2) TWICE DAILY(230/57.5 MG/M**2 ) TWICE DAILY. During the same period patient was treated with FLUTICASONE PROPIONATE, MOMETASONE FUROATE, DIDANOSINE, LAMIVUDINE, MONTELUKAST. Patient recovered.

Lopinavir Side Effects Report #5365718-5
Consumer or non-health professional from UNITED STATES reported LOPINAVIR problem on June 19, 2007. Male patient, child 9 years of age, weighting 53.57 lb, was diagnosed with hiv infection cdc category a1, asthma, rhinitis allergic and was treated with LOPINAVIR. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . LOPINAVIR dosage: 216/54 MG (230/57.5 MG/M2) TWICE DAILY(230/57.5 MG/M**2 ) TWICE DAILY. During the same period patient was treated with FLUTICASONE PROPIONATE, MOMETASONE FUROATE, DIDANOSINE, LAMIVUDINE, MONTELUKAST. Patient recovered.

Fluticasone Side Effects Report #5370966-4
FLUTICASONE PROPIONATE problem was reported by a Consumer or non-health professional from on June 20, 2007. Male patient, child 9 years of age, weighting 53.57 lb, was diagnosed with rhinitis allergic, asthma, hiv infection cdc category a1 and was treated with FLUTICASONE PROPIONATE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, cushingoid, hair growth abnormal, swelling, weight increased, . FLUTICASONE PROPIONATE dosage: unknown. During the same period patient was treated with MOMETASONE FUROATE, LOPINAVIR, DIDANOSINE, LAMIVUDINE, MONTELUKAST. Patient recovered.

Clobetasol Side Effects Report #5372962-X
Consumer or non-health professional from UNITED STATES reported CLOBETASOL PROPIONATE problem on June 14, 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: cushing's syndrome, diabetes mellitus, osteoporosis, . CLOBETASOL PROPIONATE dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Seretide Side Effects Report #5323826-9
SERETIDE problem was reported by a Consumer or non-health professional from FRANCE on May 03, 2007. Male patient, 56 years of age, was diagnosed with asthmatic crisis, hiv infection and was treated with SERETIDE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, face oedema, . SERETIDE dosage: unknown. During the same period patient was treated with SYMBICORT, KENACORT, KALETRA, VENTOLIN, TRUVADA. Patient was hospitalized. Patient recovered.

Pulmicort Side Effects Report #5325327-0
Consumer or non-health professional from NETHERLANDS reported PULMICORT problem on May 11, 2007. Female patient, 30 years of age, weighting 180.8 lb, was diagnosed with asthma and was treated with PULMICORT. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . PULMICORT dosage: unknown. Patient was hospitalized. Patient recovered.

Symbicort Side Effects Report #5327834-3
SYMBICORT problem was reported by a Health Professional from FRANCE on May 09, 2007. Male patient, 56 years of age, was diagnosed with asthma, hiv infection and was treated with SYMBICORT. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . SYMBICORT dosage: unknown. During the same period patient was treated with KENACORT, SERETIDE, KALETRA, TRUVADA. Patient was hospitalized. Patient recovered.

Flovent Side Effects Report #5304397-X
Consumer or non-health professional from UNITED STATES reported FLOVENT problem on Apr 02, 2007. Female patient, child 12 years of age, was diagnosed with wheezing, hiv infection and was treated with FLOVENT. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, weight increased, . FLOVENT dosage: unknown. Patient recovered.

Asmanex Side Effects Report #5271530-8
ASMANEX TWISTHALER problem was reported by a Physician from UNITED STATES on Mar 05, 2007. Male patient was treated with ASMANEX TWISTHALER. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . ASMANEX TWISTHALER dosage: unknown. Patient recovered.

Hydrocortone Side Effects Report #5275907-6
Health Professional from UNITED STATES reported HYDROCORTONE problem on Mar 15, 2007. Male patient, child 11 years of age, weighting 90.39 lb, was diagnosed with pruritus and was treated with HYDROCORTONE. After drug was administered, patient experienced the following problems/side effects: cushing's syndrome, . HYDROCORTONE dosage: unknown. During the same period patient was treated with AQUAPHOR OINTMENT. Patient was hospitalized. Patient recovered.

Fluticasone Side Effects Report #5663710-4
FLUTICASONE PROPIONATE problem was reported by a Consumer or non-health professional from UNITED STATES 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.

Nifedipine Side Effects Report #5670282-7
Consumer or non-health professional from JAPAN reported NIFEDIPINE problem 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.

Enbrel Side Effects Report #5621683-4
ENBREL problem was reported by a Physician from UNITED STATES 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.

Clobetasol Side Effects Report #5625260-0
Consumer or non-health professional from TURKEY reported CLOBETASOL PROPIONATE problem 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.

Kenalog Side Effects Report #5637245-9
KENALOG problem was reported by a Consumer or non-health professional from UNITED STATES 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.

Byetta Side Effects Report #5653944-7
Consumer or non-health professional from UNITED STATES reported BYETTA problem 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.

Cellcept Side Effects Report #5574623-0
CELLCEPT problem was reported by a Physician from GERMANY 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.

Hydroquinone Side Effects Report #5506174-3
Physician from BELGIUM reported HYDROQUINONE problem 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.

Clobetasol Side Effects Report #5506198-6
CLOBETASOL problem was reported by a Physician from BELGIUM 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.

Decadron Side Effects Report #5509342-X
Consumer or non-health professional from UNITED STATES reported DECADRON problem 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.

Keppra Side Effects Report #5520543-7
KEPPRA problem was reported by a Physician from UNITED STATES 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.

Decadron Side Effects Report #5523053-6
Health Professional from UNITED STATES reported DECADRON UNK problem 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.

Fluticasone Side Effects Report #5531278-9
FLUTICASONE PROPIONATE problem was reported by a Consumer or non-health professional from CANADA 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.

Temozolomide Side Effects Report #5532369-9
Physician from UNITED STATES reported TEMOZOLOMIDE problem 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.

Clobetasol Side Effects Report #5478857-5
CLOBETASOL PROPIONATE problem was reported by a Physician from TURKEY 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.

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.

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