HYPERKERATOSIS side effect
What is HYPERKERATOSIS ?Drugs associated with HYPERKERATOSIS
ADVAIR ATAZANAVIR AVONEX BONIVA BYETTA CYCLOSPORINE CYTARABINE ENBREL FLUDARABINE INTRON KENALOG LAMIVUDINE NEXAVAR PEGASYS REMICADE SORAFENIB SUTENT TERBINAFINE ZOLINZAHYPERKERATOSIS : Atazanavir Side Effects Report #5677041-X
Health Professional from UNITED STATES reported ATAZANAVIR SULPHATE problem on Mar 17, 2008. Female patient, child 5 years of age, weighting 41.89 lb, was diagnosed with hiv infection and was treated with ATAZANAVIR SULPHATE. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, skin hyperpigmentation, . ATAZANAVIR SULPHATE dosage: STARTED-}150MG: 22DEC03-25JAN05, 200MG 26JAN2005-27AUG2007, 250MG FROM 28AUG2007-}CONTINUES. Patient recovered.
HYPERKERATOSIS : Fludarabine Side Effects Report #5623330-4
FLUDARABINE problem was reported by a Health Professional from AUSTRALIA on Jan 31, 2008. Male patient, 70 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with FLUDARABINE. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, hyperkeratosis follicularis et parafollicularis, rash papular, . FLUDARABINE dosage: unknown. During the same period patient was treated with CYCLOPHOSPHAMIDE, RITUXIMAB. Patient recovered.
HYPERKERATOSIS : Pegasys Side Effects Report #5637121-1
Physician from SWITZERLAND reported PEGASYS problem on Feb 14, 2008. Male patient, 45 years of age, weighting 149.9 lb, was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, . PEGASYS dosage: unknown. During the same period patient was treated with COPEGUS. Patient recovered.
HYPERKERATOSIS : Enbrel Side Effects Report #5561053-0
ENBREL problem was reported by a Health Professional from UNITED STATES on Nov 01, 2007. Female patient was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, . ENBREL dosage: unknown. Patient recovered.
HYPERKERATOSIS : Nexavar Side Effects Report #5574545-5
Consumer or non-health professional from UNITED STATES reported NEXAVAR problem on Dec 11, 2007. Female patient, 45 years of age, was diagnosed with malignant melanoma and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, oral pain, rectal haemorrhage, tongue blistering, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. Patient recovered.
HYPERKERATOSIS : Sutent Side Effects Report #5529635-X
SUTENT problem was reported by a Health Professional from UNITED KINGDOM on Nov 20, 2007. Female patient was diagnosed with metastatic renal cell carcinoma and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, palmar-plantar erythrodysaesthesia syndrome, walking disability, . SUTENT dosage: unknown. During the same period patient was treated with ZOMETA. Patient recovered.
HYPERKERATOSIS : Avonex Side Effects Report #5483410-3
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Oct 01, 2007. Male patient, 56 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, precancerous skin lesion, . AVONEX dosage: unknown. Patient recovered.
HYPERKERATOSIS : Kenalog Side Effects Report #5493324-0
KENALOG problem was reported by a Consumer or non-health professional from UNITED STATES on May 21, 2007. Female patient was treated with KENALOG. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, inflammation, . KENALOG dosage: unknown. Patient recovered.
HYPERKERATOSIS : Avonex Side Effects Report #5384928-4
Consumer or non-health professional from UNITED STATES reported AVONEX problem on June 27, 2007. Male patient, 56 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, . AVONEX dosage: unknown. Patient recovered.
HYPERKERATOSIS : Avonex Side Effects Report #5384928-4
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on June 27, 2007. Male patient, 56 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, . AVONEX dosage: unknown. Patient recovered.
HYPERKERATOSIS : Terbinafine Side Effects Report #5657968-5
Health Professional from AUSTRIA reported TERBINAFINE problem on Feb 27, 2008. Female patient, child 12 years of age, was diagnosed with body tinea, dermatitis atopic and was treated with TERBINAFINE. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, pityriasis rubra pilaris, rash erythematous, rash pruritic, skin disorder, skin hypopigmentation, . TERBINAFINE dosage: 125 MG/DAY. During the same period patient was treated with MOMETASONE FUROATE, PIMECROLIMUS. Patient recovered.
HYPERKERATOSIS : Cyclosporine Side Effects Report #5626906-3
CYCLOSPORINE problem was reported by a Physician from UNITED KINGDOM on Feb 04, 2008. Male patient, 46 years of age, was diagnosed with renal transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: folliculitis, hyperkeratosis, skin nodule, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with PREDNISOLONE, AZATHIOPRINE, MYCOPHENOLATE MOFETIL. Patient recovered.
HYPERKERATOSIS : Intron Side Effects Report #5633066-1
Physician from FRANCE reported INTRON A problem on Feb 12, 2008. Female patient, 35 years of age, was diagnosed with malignant melanoma and was treated with INTRON A. After drug was administered, patient experienced the following problems/side effects: eczema, hyperkeratosis, pruritus, . INTRON A dosage: unknown. Patient was hospitalized. Patient recovered.
HYPERKERATOSIS : Enbrel Side Effects Report #5638272-8
ENBREL problem was reported by a Physician from FRANCE on Feb 12, 2008. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: basal cell carcinoma, hyperkeratosis, solar elastosis, . ENBREL dosage: unknown. During the same period patient was treated with NOVATREX, EUPANTOL, VOLTAREN. Patient recovered.
HYPERKERATOSIS : Lamivudine Side Effects Report #5534449-0
Consumer or non-health professional from MEXICO reported LAMIVUDINE problem on Dec 03, 2007. Male patient, 30 years of age, was diagnosed with hiv infection and was treated with LAMIVUDINE. After drug was administered, patient experienced the following problems/side effects: granuloma, hyperkeratosis, immune reconstitution syndrome, madarosis, rash, skin lesion, tuberculoid leprosy, . LAMIVUDINE dosage: 150MG PER DAY. During the same period patient was treated with ZIDOVUDINE, EFAVIRENZ. Patient recovered.
HYPERKERATOSIS : Enbrel Side Effects Report #5561895-1
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 05, 2007. Female patient was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: abscess, hyperkeratosis, . ENBREL dosage: unknown. Patient recovered.
HYPERKERATOSIS : Cytarabine Side Effects Report #5480157-4
Consumer or non-health professional from UNITED KINGDOM reported CYTARABINE problem on Aug 27, 2007. Female patient, 42 years of age, was treated with CYTARABINE. After drug was administered, patient experienced the following problems/side effects: herpes zoster, hyperkeratosis, pancytopenia, rash papular, skin necrosis, stem cell transplant, . CYTARABINE dosage: unknown. During the same period patient was treated with ETOPOSIDE, CAMPATH, CARMUSTINE, MELPHALAN, ACYCLOVIR. Patient recovered.
HYPERKERATOSIS : Nexavar Side Effects Report #5508465-9
NEXAVAR problem was reported by a Pharmacist from UNITED STATES on Aug 23, 2007. Male patient, 55 years of age, was diagnosed with hepatic cancer metastatic, metastases to lung and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: gait disturbance, hyperkeratosis, palmar-plantar erythrodysaesthesia syndrome, . NEXAVAR dosage: 400 MG, BID, ORAL ; 400 MG, QD, ORAL. During the same period patient was treated with LIPITOR. Patient recovered.
HYPERKERATOSIS : Cytarabine Side Effects Report #5470329-7
Health Professional from UNITED KINGDOM reported CYTARABINE problem on Sept 14, 2007. Female patient, 42 years of age, was diagnosed with t-cell chronic lymphocytic leukaemia and was treated with CYTARABINE. After drug was administered, patient experienced the following problems/side effects: herpes zoster, hyperkeratosis, . CYTARABINE dosage: unknown. During the same period patient was treated with ETOPOSIDE, CAMPATH, CARMUSTINE, MELPHALAN, ACYCLOVIR. Patient recovered.
HYPERKERATOSIS : Nexavar Side Effects Report #5400129-5
NEXAVAR problem was reported by a Physician from UNITED STATES on July 24, 2007. Male patient, 54 years of age, was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: anal fistula, hyperkeratosis, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. Patient recovered.
HYPERKERATOSIS : Byetta Side Effects Report #5428345-7
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Apr 30, 2007. Female patient, 63 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, hyperkeratosis, neuropathy, peripheral coldness, poor peripheral circulation, stress, . BYETTA dosage: unknown. Patient recovered.
HYPERKERATOSIS : Nexavar Side Effects Report #5400129-5
NEXAVAR problem was reported by a Physician from UNITED STATES on July 24, 2007. Male patient, 54 years of age, was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: anal fistula, hyperkeratosis, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. Patient recovered.
HYPERKERATOSIS : Byetta Side Effects Report #5428345-7
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Apr 30, 2007. Female patient, 63 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, hyperkeratosis, neuropathy, peripheral coldness, poor peripheral circulation, stress, . BYETTA dosage: unknown. Patient recovered.
HYPERKERATOSIS : Nexavar Side Effects Report #5676148-0
NEXAVAR problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 12, 2008. Female patient, 79 years of age, weighting 108.0 lb, was diagnosed with gallbladder cancer and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: blister, gait disturbance, hyperkeratosis, oral pain, pain in extremity, palmar-plantar erythrodysaesthesia syndrome, paraesthesia, tongue blistering, . NEXAVAR dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 200 MG. During the same period patient was treated with MORPHINE, VITAMINS, STOOL SOFTENER, LACTULOSE. Patient recovered.
HYPERKERATOSIS : Boniva Side Effects Report #5521838-3
Physician from UNITED STATES reported BONIVA problem on Nov 09, 2007. Female patient, 80 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: acanthosis, bone disorder, hyperkeratosis, tooth disorder, . BONIVA dosage: unknown. Patient recovered.
HYPERKERATOSIS : Advair Side Effects Report #5497677-9
ADVAIR DISKUS problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 05, 2007. Female patient was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: bone pain, headache, hyperkeratosis, joint swelling, nausea, neuralgia, oedema peripheral, pain in extremity, pharyngitis, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with PREVACID, MORPHINE. Patient recovered.
HYPERKERATOSIS : Sorafenib Side Effects Report #5508097-2
Consumer or non-health professional from UNITED STATES reported SORAFENIB problem on July 13, 2007. Female patient, 45 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with SORAFENIB. After drug was administered, patient experienced the following problems/side effects: alopecia, dry skin, hyperkeratosis, kidney infection, pruritus, . SORAFENIB dosage: 400 MG, BID, ORAL; 400 MG, BID, ORAL; 400 MG, QD, ORAL. During the same period patient was treated with NORVASC, FUROSEMIDE, ZOLOFT, POTASSIUM CHLORIDE, ACIPHEX. Patient recovered.
HYPERKERATOSIS : Nexavar Side Effects Report #5508509-4
NEXAVAR problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 14, 2007. Male patient, 57 years of age, weighting 145.0 lb, was diagnosed with hepatic neoplasm malignant and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: acne, asthenia, hyperkeratosis, increased tendency to bruise, nausea, . NEXAVAR dosage: 400 MG BID ORAL. During the same period patient was treated with LEXIVA, NORVIR, TRUVADA, ADVAIR DISKUS. Patient recovered.
HYPERKERATOSIS : Remicade Side Effects Report #5430422-1
Physician from FRANCE reported REMICADE problem on Aug 21, 2007. Female patient, 33 years of age, weighting 119.0 lb, was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: dermatitis psoriasiform, folliculitis, hyperkeratosis, neoplasm skin, rash, seborrhoeic keratosis, skin infection, . REMICADE dosage: unknown. Patient recovered.
HYPERKERATOSIS : Zolinza Side Effects Report #5447098-X
ZOLINZA problem was reported by a Physician from UNITED STATES on May 01, 2007. Female patient, 44 years of age, was diagnosed with t-cell type acute leukaemia and was treated with ZOLINZA. After drug was administered, patient experienced the following problems/side effects: dry skin, ejection fraction decreased, hyperkeratosis, oedema peripheral, skin exfoliation, . ZOLINZA dosage: 400 MG/DAILY/PO. During the same period patient was treated with ANALGESIC, ANESTHETIC. Patient recovered.