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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.

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.

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.

Nexavar Side Effects Report #5574545-5
NEXAVAR problem was reported by a Consumer or non-health professional from UNITED STATES 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.


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.

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.

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.

Isotretinoin Side Effects Report #5766508-1
ISOTRETINOIN problem was reported by a Health Professional from UNITED KINGDOM on June 05, 2008. Female patient was diagnosed with acne and was treated with ISOTRETINOIN. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, . ISOTRETINOIN dosage: unknown. Patient recovered.

Humira Side Effects Report #5768997-5
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Mar 18, 2008. Male patient, weighting 260.2 lb, was diagnosed with rheumatoid arthritis, crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, . HUMIRA dosage: unknown. Patient recovered.


Isotretinoin Side Effects Report #5772322-3
ISOTRETINOIN problem was reported by a Health Professional from UNITED KINGDOM on June 05, 2008. Male patient, 17 years of age, was diagnosed with acne, dental care and was treated with ISOTRETINOIN. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, . ISOTRETINOIN dosage: unknown. During the same period patient was treated with FLUORIDE. Patient recovered.

Zyban Side Effects Report #5781956-1
Consumer or non-health professional from NETHERLANDS reported ZYBAN problem on June 18, 2008. Male patient, 56 years of age, weighting 205.0 lb, was diagnosed with depression and was treated with ZYBAN. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, lip dry, nail disorder, rash vesicular, suicidal ideation, . ZYBAN dosage: 150MG TWICE PER DAY. During the same period patient was treated with DIAZEPAM, GLIMEPIRIDE, SIMVASTATIN. Patient recovered.

Magnevist Side Effects Report #5347434-9
MAGNEVIST problem was reported by a Physician from UNITED STATES on June 04, 2007. Female patient, weighting 303.0 lb, was diagnosed with nuclear magnetic resonance imaging brain, scan with contrast and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, neovascularisation, nephrogenic fibrosing dermopathy, skin fibrosis, skin lesion, skin nodule, . MAGNEVIST dosage: unknown. Patient recovered.

Rogaine Side Effects Report #5352138-2
Consumer or non-health professional from UNITED STATES reported ROGAINE problem on May 29, 2007. Male patient, 78 years of age, weighting 192.9 lb, was diagnosed with alopecia and was treated with ROGAINE. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, tinea infection, . ROGAINE dosage: unknown. Patient recovered.

Remicade Side Effects Report #5296362-6
REMICADE problem was reported by a Health Professional from FRANCE on Apr 02, 2007. Male patient, 46 years of age, was diagnosed with colitis ulcerative and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, trichophyton infection, . REMICADE dosage: unknown. During the same period patient was treated with ATACAND. Patient was hospitalized. Patient recovered.


Byetta Side Effects Report #5298100-X
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Apr 09, 2007. Male patient, 65 years of age, weighting 250.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, localised infection, skin ulcer, . BYETTA dosage: unknown. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5302882-8
REMICADE problem was reported by a Health Professional from FRANCE on Apr 12, 2007. Male patient, 46 years of age, was diagnosed with colitis ulcerative and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, trichophyton infection, . REMICADE dosage: unknown. During the same period patient was treated with ATACAND. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5310916-X
Health Professional from FRANCE reported REMICADE problem on Apr 19, 2007. Male patient, 46 years of age, was diagnosed with colitis ulcerative and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, trichophyton infection, . REMICADE dosage: unknown. During the same period patient was treated with ATACAND. Patient was hospitalized. Patient recovered.

Terbinafine Side Effects Report #5657968-5
TERBINAFINE problem was reported by a Health Professional from AUSTRIA 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.

Cyclosporine Side Effects Report #5626906-3
Physician from UNITED KINGDOM reported CYCLOSPORINE problem 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.


Intron Side Effects Report #5633066-1
INTRON A problem was reported by a Physician from FRANCE 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.

Enbrel Side Effects Report #5638272-8
Physician from FRANCE reported ENBREL problem 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.

Lamivudine Side Effects Report #5534449-0
LAMIVUDINE problem was reported by a Consumer or non-health professional from MEXICO 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.

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.

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.

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.

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.

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.

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.

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.

Atazanavir Side Effects Report #5773724-1
ATAZANAVIR SULPHATE problem was reported by a Health Professional from UNITED STATES on June 12, 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: acanthosis nigricans, hyperkeratosis, skin hyperpigmentation, . ATAZANAVIR SULPHATE dosage: STARTED-}150MG: 22DEC03-25JAN05, 200MG 26JAN2005-27AUG2007, 250MG FROM 28AUG2007-}CONTINUES. Patient recovered.

Lucentis Side Effects Report #5729344-8
Physician from SWITZERLAND reported LUCENTIS problem on Apr 28, 2008. Female patient, 77 years of age, was treated with LUCENTIS. After drug was administered, patient experienced the following problems/side effects: erysipelas, hyperkeratosis, rash erythematous, skin fissures, . LUCENTIS dosage: unknown. During the same period patient was treated with ZOCOR, VASTAREL, CATAPRES, MICARDIS, BIPRETERAX. Patient recovered.

Atazanavir Side Effects Report #5705666-1
ATAZANAVIR SULPHATE problem was reported by a Health Professional from UNITED STATES on Apr 08, 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: acanthosis nigricans, hyperkeratosis, keratosis pilaris, skin hyperpigmentation, . ATAZANAVIR SULPHATE dosage: STARTED-}150MG: 22DEC03-25JAN05, 200MG 26JAN2005-27AUG2007, 250MG FROM 28AUG2007-}CONTINUES. Patient recovered.

Remicade Side Effects Report #5359969-3
Physician from FRANCE reported REMICADE problem on June 05, 2007. Male patient, 74 years of age, weighting 163.1 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: diffuse large b-cell lymphoma, hyperkeratosis, . REMICADE dosage: unknown. During the same period patient was treated with METHOTREXATE, IRBESARTAN, ALLOPURINOL, CALCIT D, PARACETAMOL, NEXIUM. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5324876-9
REMICADE problem was reported by a Health Professional from FRANCE on May 04, 2007. Male patient, 46 years of age, was diagnosed with colitis ulcerative and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: dermatitis psoriasiform, hyperkeratosis, trichophyton infection, . REMICADE dosage: unknown. During the same period patient was treated with ATACAND. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5336731-9
Physician from ARGENTINA reported GLEEVEC problem on May 16, 2007. Female patient, 52 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: alopecia, hyperkeratosis, skin exfoliation, . GLEEVEC dosage: 400 MG, QD. Patient recovered.

Zolinza Side Effects Report #5349551-6
ZOLINZA problem was reported by a Health Professional from UNITED STATES on Jan 29, 2007. Male patient, 78 years of age, weighting 163.0 lb, was diagnosed with t-cell lymphoma and was treated with ZOLINZA. After drug was administered, patient experienced the following problems/side effects: erythema, hyperkeratosis, pain, . ZOLINZA dosage: 400MG/DAILY/PO. Patient recovered.

Altace Side Effects Report #5292306-1
Consumer or non-health professional from FRANCE reported ALTACE problem on Mar 29, 2007. Female patient was diagnosed with chronic myeloid leukaemia and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, mycosis fungoides, pruritus, rash erythematous, rash papular, . ALTACE dosage: 1.25 MG, QD. During the same period patient was treated with LOGIMAX, ALDACTONE, MODAMIDE, KARDEGIC, GLEEVEC, URION, MAG, NUCTALON. Patient was hospitalized. Patient recovered.

Altace Side Effects Report #5293322-6
ALTACE problem was reported by a Consumer or non-health professional from FRANCE on Mar 29, 2007. Female patient was diagnosed with chronic myeloid leukaemia and was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: hyperkeratosis, lichenoid keratosis, mycosis fungoides, prurigo, pruritus, rash erythematous, rash papular, . ALTACE dosage: 1.25 MG, QD. During the same period patient was treated with KARDEGIC, ALDACTONE, MODAMIDE, GLEEVEC, LOGIMAX, URION, MAG, NUCTALON. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5306380-7
Physician from UNITED STATES reported HUMIRA problem on Apr 16, 2007. Female patient, weighting 130.1 lb, was diagnosed with rheumatoid arthritis, pain, blood pressure and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthritis, hyperkeratosis, . HUMIRA dosage: unknown. During the same period patient was treated with VICODIN, METHOTREXATE, FOLATE, RISEDRONATE, ATENOLOL, AMLODIPINE BESYLATE. Patient recovered.

Nexavar Side Effects Report #5323004-3
NEXAVAR problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 10, 2006. Male patient, 68 years of age, was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: diarrhoea, hyperkeratosis, hypertension, pain in extremity, rash, skin lesion, . NEXAVAR dosage: unknown. Patient recovered.

Quilonum Side Effects Report #5253152-8
Physician from GERMANY reported QUILONUM RETARD problem on Feb 27, 2007. Male patient, 49 years of age, weighting 196.2 lb, was diagnosed with affect lability, thinking abnormal and was treated with QUILONUM RETARD. After drug was administered, patient experienced the following problems/side effects: erythema, hyperkeratosis, psoriasis, skin fissures, . QUILONUM RETARD dosage: unknown. During the same period patient was treated with QUETIAPINE FUMARATE. Patient recovered.

Avonex Side Effects Report #5259826-7
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 23, 2007. Female patient, 66 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: arthritis, hyperkeratosis, hypertension, intervertebral discitis, meningitis bacterial, multiple sclerosis relapse, rash, renal failure acute, staphylococcal infection, . AVONEX dosage: unknown. During the same period patient was treated with BACLOFEN, LIDOCAINE, CARDIZEM CD, ALTACE, HYDROCHLOROTHIAZIDE, FOLIC ACID, NEURONTIN. Patient was hospitalized. Patient recovered.

Nicorette Side Effects Report #5260250-1
Consumer or non-health professional from UNITED STATES reported NICORETTE problem on May 26, 2006. Male patient, 49 years of age, was treated with NICORETTE. After drug was administered, patient experienced the following problems/side effects: gingival discolouration, hyperkeratosis, . NICORETTE dosage: unknown. Patient recovered.

Iressa Side Effects Report #5263494-8
IRESSA problem was reported by a Physician from UNITED STATES on Oct 11, 2004. Female patient was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: herpes zoster, hyperkeratosis, . IRESSA dosage: 250 MG DAILY. Patient recovered.

Iressa Side Effects Report #5263746-1
Physician from UNITED STATES reported IRESSA problem on Apr 07, 2005. Female patient was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: herpes zoster, hyperkeratosis, impaired healing, . IRESSA dosage: 250 MG DAILY. Patient recovered.

Iressa Side Effects Report #5264018-1
IRESSA problem was reported by a Physician from UNITED STATES on Apr 07, 2005. Female patient was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: herpes zoster, hyperkeratosis, impaired healing, . IRESSA dosage: 250 MG DAILY. Patient recovered.

Humira Side Effects Report #5267565-1
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Mar 07, 2007. Female patient, weighting 130.1 lb, was diagnosed with rheumatoid arthritis, pain, blood pressure and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthritis, hyperkeratosis, . HUMIRA dosage: unknown. During the same period patient was treated with VICODIN. Patient recovered.

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.

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.

Sorafenib Side Effects Report #5508097-2
SORAFENIB problem was reported by a Consumer or non-health professional from UNITED STATES 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.

Nexavar Side Effects Report #5508509-4
Consumer or non-health professional from UNITED STATES reported NEXAVAR problem 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.