KETODERM Side Effects

6723188-6 | Application Site Reaction
on May 05, 2010 Male patient from FRANCE , weighting 286.6 lb, was treated with Ketoderm (View Usage). Patient experienced the following unwanted or unexpected effects: application site reaction. Ketoderm dosage: . During the same period patient was treated with COKENZEN (View Cokenzen Review and Cokenzen Label ), GLICLAZIDE (View Gliclazide Review and Gliclazide Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), TAHOR (View Tahor Review and Tahor Label ), FLUINDIONE (View Fluindione Review and Fluindione Label ).

6422767-3 | Anaemia, Dyshidrosis, Eczema, Eosinophilia, Type Iv Hypersensitivity Reaction
Patient was taking Ketoderm (View Usage). Patient had the following side effects: anaemia, dyshidrosis, eczema (What is eczema?), eosinophilia, type iv hypersensitivity reaction on Oct 23, 2009 from FRANCE Additional patient health information: Female patient , weighting 134.5 lb, was diagnosed with dermatitis and. Ketoderm dosage: . During the same period patient was treated with ECONAZOLE NITRATE (View Econazole Nitrate Review and Econazole Nitrate Label ), PYOSTACINE (View Pyostacine Review and Pyostacine Label ), BETADINE (View Betadine Review and Betadine Label ). Patient was hospitalized.

6216094-7 | Anaemia, Dyshidrosis, Eczema, Eosinophilia, Type Iv Hypersensitivity Reaction
Adverse event was reported on May 28, 2009 by a Female patient taking Ketoderm (View Usage) (Dosage: ) was diagnosed with dermatitis and. Location: FRANCE , weighting 134.5 lb, After Ketoderm was administered, patient had the following side effects: anaemia, dyshidrosis, eczema (What is eczema?), eosinophilia, type iv hypersensitivity reaction. During the same period patient was treated with PYOSTACINE (View Pyostacine Review and Pyostacine Label ), ECONAZOLE NITRATE (View Econazole Nitrate Review and Econazole Nitrate Label ), BETADINE (View Betadine Review and Betadine Label ). Patient was hospitalized.

6169966-6 | Genital Burning Sensation, Skin Exfoliation
on Apr 22, 2009 Female patient from FRANCE , weighting 22.05 lb, was diagnosed with dermatitis diaper and was treated with Ketoderm (View Usage). Patient experienced the following unwanted or unexpected effects: genital burning sensation, skin exfoliation. Ketoderm dosage: .


5948707-9 | Diarrhoea, Hypovolaemic Shock, Hypoxia, Vomiting
on Oct 06, 2008 Male patient from FRANCE , weighting 187.4 lb, was diagnosed with tinea versicolour and was treated with Ketoderm (View Usage). Patient had the following side effects: diarrhoea, hypovolaemic shock, hypoxia, vomiting. Ketoderm dosage: . During the same period patient was treated with ZESTRIL (View Zestril Review and Zestril Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), CALCIUM D3 (View Calcium D3 Review and Calcium D3 Label ), MOPRAL (View Mopral Review and Mopral Label ), SEREVENT (View Serevent Review and Serevent Label ). Patient was hospitalized.

5918454-8 | Diarrhoea, Hypovolaemic Shock, Hypoxia, Vomiting
Patient was taking Ketoderm (View Usage). After Ketoderm was administered, patient had the following side effects: diarrhoea, hypovolaemic shock, hypoxia, vomiting on Oct 06, 2008 from FRANCE Additional patient health information: Male patient , weighting 187.4 lb, was diagnosed with tinea versicolour and. Ketoderm dosage: . During the same period patient was treated with ZESTRIL (View Zestril Review and Zestril Label ), CORTANCYL (View Cortancyl Review and Cortancyl Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), CALCIUM D3 (View Calcium D3 Review and Calcium D3 Label ), MOPRAL (View Mopral Review and Mopral Label ), SEREVENT (View Serevent Review and Serevent Label ). Patient was hospitalized.

5726207-9 | Asthma
Adverse event was reported on Apr 24, 2008 by a Female patient taking Ketoderm (View Usage) (Dosage: ) was diagnosed with fungal infection (What is fungal infection?) and. Location: FRANCE , weighting 127.9 lb, Patient experienced the following unwanted or unexpected effects: asthma (What is asthma?). During the same period patient was treated with HALDOL (View Haldol Review and Haldol Label ).

5697584-2 | Asthma
on Apr 03, 2008 Female patient from FRANCE , 55 years of age, was diagnosed with fungal infection (What is fungal infection?) and was treated with Ketoderm (View Usage). Patient had the following side effects: asthma (What is asthma?). Ketoderm dosage: .

5301707-4 | Burkitt's Lymphoma, Cytomegalovirus Test Positive, Lymphocytosis, Neutropenia, Oesophagitis Ulcerative, Renal Failure Acute, Tendonitis
on Apr 06, 2007 Male patient from , 49 years of age, weighting 165.3 lb, was diagnosed with seborrhoeic dermatitis, gastrointestinal disorder, prophylaxis, hyperuricaemia and was treated with Ketoderm (View Usage). After Ketoderm was administered, patient had the following side effects: burkitt's lymphoma, cytomegalovirus test positive, lymphocytosis, neutropenia, oesophagitis ulcerative, renal failure acute, tendonitis. Ketoderm dosage: . During the same period patient was treated with DEBRIDAT ^IBRAHIM^ (View Debridat ^ibrahim^ Review and Debridat ^ibrahim^ Label ), BACTRIM (480 Mg, Unk) (View Bactrim Review and Bactrim Label ), FASTURTEC (View Fasturtec Review and Fasturtec Label ), SOLU MEDROL (40 Mg, Thrice) (View Solu-medrol Review and Solu-medrol Label ), DEPO MEDROL (View Depo-medrol Review and Depo-medrol Label ), DEPO MEDROL (View Depo-medrol Review and Depo-medrol Label ), ARACYTIN (View Aracytin Review and Aracytin Label ), METHOTREXATE (Unk, Unk) (View Methotrexate Review and Methotrexate Label ). Patient was hospitalized.

5232259-5 | Burkitt's Lymphoma, Cytomegalovirus Test Positive, Lymphocytosis, Neutropenia, Oesophagitis Ulcerative, Renal Failure Acute, Tendonitis
Patient was taking Ketoderm (View Usage). Patient experienced the following unwanted or unexpected effects: burkitt's lymphoma, cytomegalovirus test positive, lymphocytosis, neutropenia, oesophagitis ulcerative, renal failure acute, tendonitis on Jan 26, 2007 from Additional patient health information: Male patient , 49 years of age, weighting 165.3 lb, was diagnosed with seborrhoeic dermatitis, gastrointestinal disorder, prophylaxis, hyperuricaemia and. Ketoderm dosage: . During the same period patient was treated with DEBRIDAT ^IBRAHIM^ (View Debridat ^ibrahim^ Review and Debridat ^ibrahim^ Label ), BACTRIM (480 Mg, Unk) (View Bactrim Review and Bactrim Label ), FASTURTEC (View Fasturtec Review and Fasturtec Label ), SOLU MEDROL (40 Mg, Thrice) (View Solu-medrol Review and Solu-medrol Label ), DEPO MEDROL (View Depo-medrol Review and Depo-medrol Label ), DEPO MEDROL (View Depo-medrol Review and Depo-medrol Label ), ARACYTIN (View Aracytin Review and Aracytin Label ), METHOTREXATE (Unk, Unk) (View Methotrexate Review and Methotrexate Label ). Patient was hospitalized.

5117184-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Bilirubin Unconjugated, Chromaturia, Faeces Discoloured, Gamma-glutamyltransferase Increased
Adverse event was reported on Aug 21, 2006 by a Male patient taking Ketoderm (View Usage) (Dosage: ) was diagnosed with intertrigo, urinary tract infection (What is urinary tract infection?), tinea cruris and. Location: FRANCE , 45 years of age, Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated, chromaturia, faeces discoloured, gamma-glutamyltransferase increased. During the same period patient was treated with CIFLOX (View Ciflox Review and Ciflox Label ), BACTRIM (2 Df, Qd) (View Bactrim Review and Bactrim Label ), LAMISIL (500 Mg/day) (View Lamisil Review and Lamisil Label ). Patient was hospitalized.

5009432-4 | Application Site Photosensitivity Reaction
on May 18, 2006 Female patient from FRANCE , 37 years of age, was diagnosed with hiv infection (What is hiv infection?) and was treated with Ketoderm (View Usage). After Ketoderm was administered, patient had the following side effects: application site photosensitivity reaction. Ketoderm dosage: . During the same period patient was treated with TRIZIVIR (View Trizivir Review and Trizivir Label ), LOCAL CORTICOSTEROIDS (View Local Corticosteroids Review and Local Corticosteroids Label ). Patient was hospitalized.

4868082-0 | Face Oedema, Pruritus, Rash Erythematous
on Dec 19, 2005 Female patient from FRANCE , 54 years of age, was treated with Ketoderm (View Usage). Patient experienced the following unwanted or unexpected effects: face oedema, pruritus, rash erythematous. Ketoderm dosage: . During the same period patient was treated with DUPHASTON (View Duphaston Review and Duphaston Label ), ESTREVA (View Estreva Review and Estreva Label ).