MICONAZOLE Side Effects

7006534-8 | Vulvovaginal Burning Sensation, Vulvovaginal Pain, Vulvovaginal Pruritus
on Sep 21, 2010 Female patient from UNITED STATES , 37 years of age, weighting 130.0 lb, was diagnosed with fungal infection (What is fungal infection?) and was treated with Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: vulvovaginal burning sensation, vulvovaginal pain, vulvovaginal pruritus. Miconazole dosage: 1200mg 1 Vag.

6861438-6 | Serotonin Syndrome
Patient was taking Miconazole (View Usage). Patient had the following side effects: serotonin syndrome on Jun 30, 2010 from FRANCE Additional patient health information: Female patient , 82 years of age, was diagnosed with oral candidiasis and. Miconazole dosage: 50 Mg Once A Day Buccal. During the same period patient was treated with ESCITALOPRAM (View Escitalopram Review and Escitalopram Label ). Patient was hospitalized.

6430015-3 | Haematuria, Haemorrhage Subcutaneous, Swelling
Adverse event was reported on Oct 28, 2009 by a Male patient taking Miconazole (View Usage) (Dosage: ) was diagnosed with oral candidiasis, atrial fibrillation (What is atrial fibrillation?), hyperlipidaemia and. Location: JAPAN , weighting 121.3 lb, After Miconazole was administered, patient had the following side effects: haematuria, haemorrhage subcutaneous, swelling. During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ROSUVASTATIN CALCIUM (View Rosuvastatin Calcium Review and Rosuvastatin Calcium Label ), PILSICAINIDE HYDROCHLORIDE (View Pilsicainide Hydrochloride Review and Pilsicainide Hydrochloride Label ). Patient was hospitalized.

6399588-3 | Haematuria, Haemorrhage Subcutaneous, Swelling
on Oct 05, 2009 Male patient from JAPAN , weighting 121.3 lb, was diagnosed with oral candidiasis, atrial fibrillation (What is atrial fibrillation?) and was treated with Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: haematuria, haemorrhage subcutaneous, swelling. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ROSUVASTATIN CALCIUM (View Rosuvastatin Calcium Review and Rosuvastatin Calcium Label ), PILSICAINIDE HYDROCHLORIDE (View Pilsicainide Hydrochloride Review and Pilsicainide Hydrochloride Label ). Patient was hospitalized.


6395249-5 | Stevens-johnson Syndrome
on Oct 02, 2009 Female patient from JAPAN , 28 years of age, was treated with Miconazole (View Usage). Patient had the following side effects: stevens-johnson syndrome. Miconazole dosage: .

6395247-1 | Mouth Haemorrhage, Prothrombin Time Prolonged
Patient was taking Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: mouth haemorrhage, prothrombin time prolonged on Sep 30, 2009 from JAPAN Additional patient health information: Male patient , 58 years of age, weighting 158.7 lb, was diagnosed with oral candidiasis, thrombosis prophylaxis and. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ).

6256902-7 | Haematocrit Decreased, Haemoglobin Decreased, Haemorrhage Subcutaneous, International Normalised Ratio Increased, Mouth Haemorrhage, Red Blood Cell Count Decreased
Adverse event was reported on Jun 29, 2009 by a Female patient taking Miconazole (View Usage) (Dosage: ) was diagnosed with oral fungal infection, prophylaxis, cardiac failure, parkinson's disease (What is parkinson's disease?) and. Location: JAPAN , weighting 119.0 lb, Patient experienced the following unwanted or unexpected effects: haematocrit decreased, haemoglobin decreased, haemorrhage subcutaneous, international normalised ratio increased, mouth haemorrhage, red blood cell count decreased. During the same period patient was treated with WARFARIN (View Warfarin Review and Warfarin Label ), LASIX (View Lasix Review and Lasix Label ), CARBIDOPA AND LEVODOPA (View Carbidopa And Levodopa Review and Carbidopa And Levodopa Label ), DOPS (View Dops Review and Dops Label ), REQUIP (View Requip Review and Requip Label ), SELEGILINE HCL (View Selegiline Hcl Review and Selegiline Hcl Label ). Patient was hospitalized.

6246256-4 | International Normalised Ratio Increased
on Jun 18, 2009 Male patient from UNITED KINGDOM , 74 years of age, weighting 157.0 lb, was diagnosed with oral fungal infection, atrial fibrillation (What is atrial fibrillation?), haemorrhoids, myocardial ischaemia, hypercholesterolaemia, dry skin and was treated with Miconazole (View Usage). Patient had the following side effects: international normalised ratio increased. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ANUSOL HC (View Anusol Hc Review and Anusol Hc Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), CHLORAMPHENICOL (View Chloramphenicol Review and Chloramphenicol Label ), EMOLLIENTS AND PROTECTIVES (View Emollients And Protectives Review and Emollients And Protectives Label ). Patient was hospitalized.

6241088-5 | International Normalised Ratio Increased
on Jun 16, 2009 Female patient from UNITED KINGDOM , 81 years of age, weighting 121.3 lb, was diagnosed with oral candidiasis and was treated with Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: international normalised ratio increased. Miconazole dosage: . During the same period patient was treated with WARFARIN (View Warfarin Review and Warfarin Label ), ERYTHROMYCIN (View Erythromycin Review and Erythromycin Label ). Patient was hospitalized.

6236881-9 | International Normalised Ratio Increased
Patient was taking Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased on Jun 16, 2009 from UNITED KINGDOM Additional patient health information: Female patient , 81 years of age, weighting 121.3 lb, was diagnosed with oral candidiasis and. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ERYTHROMYCIN (View Erythromycin Review and Erythromycin Label ). Patient was hospitalized.

6232475-X | Haemorrhage Subcutaneous, Mouth Haemorrhage
Adverse event was reported on Jun 09, 2009 by a Female patient taking Miconazole (View Usage) (Dosage: ) was diagnosed with oral fungal infection, prophylaxis, cardiac failure, parkinson's disease (What is parkinson's disease?) and. Location: JAPAN , weighting 119.0 lb, Patient had the following side effects: haemorrhage subcutaneous, mouth haemorrhage. During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), LASIX (View Lasix Review and Lasix Label ), CARBIDOPA AND LEVODOPA (View Carbidopa And Levodopa Review and Carbidopa And Levodopa Label ), DOPS (View Dops Review and Dops Label ), REQUIP (View Requip Review and Requip Label ), SELEGILINE HCL (View Selegiline Hcl Review and Selegiline Hcl Label ). Patient was hospitalized.

6219599-8 | Gastrointestinal Haemorrhage, International Normalised Ratio Increased
on Jun 05, 2009 Female patient from JAPAN , 80 years of age, weighting 74.96 lb, was diagnosed with oral candidiasis, atrial fibrillation (What is atrial fibrillation?) and was treated with Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: gastrointestinal haemorrhage, international normalised ratio increased. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), CALCITRIOL (View Calcitriol Review and Calcitriol Label ), FAMOTIDINE (View Famotidine Review and Famotidine Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), VITAMIN E (View Vitamin E Review and Vitamin E Label ), ISOSORBIDE MONONITRATE (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), MECOBALAMIN (View Mecobalamin Review and Mecobalamin Label ). Patient was hospitalized.

6208669-6 | International Normalised Ratio Increased
on May 28, 2009 Female patient from UNITED KINGDOM , 72 years of age, was treated with Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased. Miconazole dosage: . During the same period patient was treated with ACYCLOVIR (View Acyclovir Review and Acyclovir Label ), CHOLINE SALICYLATE (View Choline Salicylate Review and Choline Salicylate Label ).

6208646-5 | Gastrointestinal Haemorrhage, International Normalised Ratio Increased
Patient was taking Miconazole (View Usage). Patient had the following side effects: gastrointestinal haemorrhage, international normalised ratio increased on May 25, 2009 from JAPAN Additional patient health information: Female patient , 80 years of age, weighting 74.96 lb, was diagnosed with oral candidiasis, atrial fibrillation (What is atrial fibrillation?) and. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), CALCITRIOL (View Calcitriol Review and Calcitriol Label ), FAMOTIDINE (View Famotidine Review and Famotidine Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), VITAMIN E (View Vitamin E Review and Vitamin E Label ), ISOSORBIDE MONONITRATE (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), MECOBALAMIN (View Mecobalamin Review and Mecobalamin Label ). Patient was hospitalized.

6087632-2 | Contusion, International Normalised Ratio Increased
Adverse event was reported on Feb 12, 2009 by a Male patient taking Miconazole (View Usage) (Dosage: ) was diagnosed with oesophageal candidiasis and. Location: JAPAN , 68 years of age, After Miconazole was administered, patient had the following side effects: contusion, international normalised ratio increased. During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ). Patient was hospitalized.

6071577-8 | Haemorrhage, Pain, Product Quality Issue
on Feb 05, 2009 Female patient from UNITED STATES , child 7 years of age, was treated with Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: haemorrhage, pain (What is pain?), product quality issue. Miconazole dosage: .

5990166-4 | Visual Impairment
on Nov 28, 2008 Female patient from UNITED KINGDOM , 43 years of age, weighting 211.6 lb, was diagnosed with hypertension and was treated with Miconazole (View Usage). Patient had the following side effects: visual impairment. Miconazole dosage: . During the same period patient was treated with PERINDOPRIL (Daily Dose: 4 Milligram(s)) (View Perindopril Review and Perindopril Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ).

5961507-9 | Conjunctival Haemorrhage, International Normalised Ratio Increased
Patient was taking Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: conjunctival haemorrhage, international normalised ratio increased on Nov 13, 2007 from JAPAN Additional patient health information: Female patient , 78 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ATORVASTATIN CALCIUM HYDRATE (View Atorvastatin Calcium Hydrate Review and Atorvastatin Calcium Hydrate Label ).

5798306-7 | Haematuria, Haemorrhage Subcutaneous
Adverse event was reported on Jul 02, 2008 by a Female patient taking Miconazole (View Usage) (Dosage: ) . Location: JAPAN , 68 years of age, Patient experienced the following unwanted or unexpected effects: haematuria, haemorrhage subcutaneous. During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ).

5747384-X | International Normalised Ratio Increased, Purpura, Rash, Retinal Haemorrhage
on May 12, 2008 Female patient from JAPAN , 86 years of age, was diagnosed with oral candidiasis, angina pectoris and was treated with Miconazole (View Usage). Patient had the following side effects: international normalised ratio increased, purpura, rash (What is rash?), retinal haemorrhage. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ).

5684467-7 | Contusion, International Normalised Ratio Increased
on Mar 19, 2008 Female patient from UNITED KINGDOM , 71 years of age, weighting 213.8 lb, was diagnosed with oral candidiasis, atrial fibrillation (What is atrial fibrillation?), hyperthyroidism, cardiac failure congestive, depression (What is depression?), mania and was treated with Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: contusion, international normalised ratio increased. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ACETAMINOPHEN W/ PROPOXYPHENE HCL (View Acetaminophen W/ Propoxyphene Hcl Review and Acetaminophen W/ Propoxyphene Hcl Label ), CARBIMAZOLE (View Carbimazole Review and Carbimazole Label ), CO AMILOFRUSE (View Co-amilofruse Review and Co-amilofruse Label ), ELANTAN LA (View Elantan La Review and Elantan La Label ), FLUOXETINE (View Fluoxetine Review and Fluoxetine Label ), PRIADEL (View Priadel Review and Priadel Label ). Patient was hospitalized.

5683822-9 | Haematuria, International Normalised Ratio Increased
Patient was taking Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: haematuria, international normalised ratio increased on Mar 19, 2008 from UNITED KINGDOM Additional patient health information: Female patient , 73 years of age, was diagnosed with oral candidiasis and. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), ANGITIL (View Angitil Review and Angitil Label ). Patient was hospitalized.

5521795-X | Blood Calcium Decreased, Confusional State, International Normalised Ratio Increased, Somnolence
Adverse event was reported on Nov 09, 2007 by a Female patient taking Miconazole (View Usage) (Dosage: ) was diagnosed with parkinson's disease (What is parkinson's disease?) and. Location: UNITED KINGDOM , 84 years of age, Patient had the following side effects: blood calcium decreased, confusional state, international normalised ratio increased, somnolence. During the same period patient was treated with NITROFURANTOIN (View Nitrofurantoin Review and Nitrofurantoin Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), LAMOTRIGINE (View Lamotrigine Review and Lamotrigine Label ), CALCIUM (View Calcium Review and Calcium Label ), COLECALCIFEROL (View Colecalciferol Review and Colecalciferol Label ).

5476724-4 | Application Site Irritation, Application Site Pain, Application Site Pruritus
on Oct 02, 2007 Female patient from UNITED STATES , 60 years of age, weighting 258.0 lb, was diagnosed with fungal infection (What is fungal infection?) and was treated with Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: application site irritation, application site pain, application site pruritus. Miconazole dosage: There Were 3 Dose''s Once A Night Vag.

5407080-5 | Blood Bilirubin Increased, Blood Urea Increased, Haemoglobin Decreased, Sepsis, White Blood Cell Count Decreased
on Jul 27, 2007 Male patient from JAPAN , 67 years of age, was diagnosed with gastrointestinal fungal infection and was treated with Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: blood bilirubin increased, blood urea increased, haemoglobin decreased, sepsis (What is sepsis?), white blood cell count decreased. Miconazole dosage: . During the same period patient was treated with CEFOTAXIME SODIUM (View Cefotaxime Sodium Review and Cefotaxime Sodium Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), METHYPHENIDATE HYDROCHLORIDE (View Methyphenidate Hydrochloride Review and Methyphenidate Hydrochloride Label ).

5397534-2 | Phlebitis
Patient was taking Miconazole (View Usage). Patient had the following side effects: phlebitis on Jul 19, 2007 from JAPAN Additional patient health information: Female patient , weighting 103.6 lb, was diagnosed with candidiasis, iron deficiency anaemia and. Miconazole dosage: . During the same period patient was treated with FERRIC OXIDE SACCHARATED (View Ferric Oxide Saccharated Review and Ferric Oxide Saccharated Label ).

5396555-3 | Bilirubinuria, Blood Bilirubin Increased, Blood Creatinine Increased, Blood Urea Increased, Haemoglobin Decreased, White Blood Cell Count Decreased
Adverse event was reported on Jul 17, 2007 by a Male patient taking Miconazole (View Usage) (Dosage: ) was diagnosed with gastrointestinal fungal infection and. Location: JAPAN , 67 years of age, After Miconazole was administered, patient had the following side effects: bilirubinuria, blood bilirubin increased, blood creatinine increased, blood urea increased, haemoglobin decreased, white blood cell count decreased. During the same period patient was treated with CEFOTAXIME SODIUM (View Cefotaxime Sodium Review and Cefotaxime Sodium Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), METHYPHENIDATE HYDROCHLORIDE (View Methyphenidate Hydrochloride Review and Methyphenidate Hydrochloride Label ).

5392000-2 | Haematuria
on Jul 11, 2007 Female patient from JAPAN , 64 years of age, was diagnosed with oral candidiasis and was treated with Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: haematuria. Miconazole dosage: . During the same period patient was treated with BETAMETHASONE D CHLORPHENIRAMINE MALEATE (View Betamethasone-d-chlorpheniramine Maleate Review and Betamethasone-d-chlorpheniramine Maleate Label ), OLOPATADINE HYDROCHLORIDE (View Olopatadine Hydrochloride Review and Olopatadine Hydrochloride Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), THEOPHYLLINE (View Theophylline Review and Theophylline Label ), AMBROXOL HYDROCHLORIDE (View Ambroxol Hydrochloride Review and Ambroxol Hydrochloride Label ), TRAMAZOLINE HYDROCHLORIDE (View Tramazoline Hydrochloride Review and Tramazoline Hydrochloride Label ), FLUOROMETHOLONE (View Fluorometholone Review and Fluorometholone Label ).

5341809-X | Haemorrhagic Diathesis
on May 23, 2007 Female patient from JAPAN , weighting 98.33 lb, was diagnosed with gastrointestinal candidiasis, atrial fibrillation (What is atrial fibrillation?), hyperlipidaemia, diabetes mellitus, gastric ulcer, constipation (What is constipation?) and was treated with Miconazole (View Usage). Patient had the following side effects: haemorrhagic diathesis. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), PRAVASTATIN SODIUM (View Pravastatin Sodium Review and Pravastatin Sodium Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), NATEGLINIDE (View Nateglinide Review and Nateglinide Label ), DIMETICONE (View Dimeticone Review and Dimeticone Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ), FAMOTIDINE (View Famotidine Review and Famotidine Label ). Patient was hospitalized.

5328342-6 | Anaphylactic Reaction
Patient was taking Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: anaphylactic reaction on May 15, 2007 from BELGIUM Additional patient health information: Female patient , 33 years of age, was diagnosed with vaginal candidiasis and. Miconazole dosage: . Patient was hospitalized.

5283420-5 | Gingival Bleeding, Haemorrhage Subcutaneous, Lip Haemorrhage
Adverse event was reported on Mar 22, 2007 by a Female patient taking Miconazole (View Usage) (Dosage: ) was diagnosed with oral candidiasis, hyperlipidaemia, pulmonary hypertension (What is pulmonary hypertension?), reflux oesophagitis, diabetes mellitus and. Location: JAPAN , weighting 79.81 lb, Patient experienced the following unwanted or unexpected effects: gingival bleeding, haemorrhage subcutaneous, lip haemorrhage. During the same period patient was treated with ROSUVASTATIN CALCIUM (View Rosuvastatin Calcium Review and Rosuvastatin Calcium Label ), WARFARIN POTASSIUM (View Warfarin Potassium Review and Warfarin Potassium Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), RABEPRAZOLE SODIUM (View Rabeprazole Sodium Review and Rabeprazole Sodium Label ), BERAPROST SODIUM (View Beraprost Sodium Review and Beraprost Sodium Label ), ACARBOSE (View Acarbose Review and Acarbose Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ). Patient was hospitalized.

5283419-9 | Haemorrhagic Diathesis
on Mar 23, 2007 Female patient from JAPAN , weighting 98.33 lb, was diagnosed with gastrointestinal candidiasis, atrial fibrillation (What is atrial fibrillation?), gastric ulcer and was treated with Miconazole (View Usage). Patient had the following side effects: haemorrhagic diathesis. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), PRAVASTATIN SODIUM (View Pravastatin Sodium Review and Pravastatin Sodium Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), NATEGLINIDE (View Nateglinide Review and Nateglinide Label ), DIMETICONE (View Dimeticone Review and Dimeticone Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ), FAMOTIDINE (View Famotidine Review and Famotidine Label ). Patient was hospitalized.

5268987-5 | Mouth Haemorrhage, Petechiae
on Mar 07, 2007 Female patient from JAPAN , 54 years of age, was diagnosed with oral candidiasis, hyperlipidaemia and was treated with Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: mouth haemorrhage, petechiae. Miconazole dosage: . During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ROSUVASTATIN CALCIUM (View Rosuvastatin Calcium Review and Rosuvastatin Calcium Label ), PRENISOLONE (View Prenisolone Review and Prenisolone Label ). Patient was hospitalized.

5197715-7 | Blood Creatine Phosphokinase Increased, Liver Function Test Abnormal
Patient was taking Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, liver function test abnormal on Dec 20, 2006 from JAPAN Additional patient health information: Female patient , 81 years of age, was diagnosed with oral candidiasis and. Miconazole dosage: .

5103597-1 | Abdominal Distension, Abdominal Pain, Constipation, Rash, Skin Ulcer, Vaginal Haemorrhage
Adverse event was reported on Sep 08, 2006 by a Female patient taking Miconazole (View Usage) (Dosage: 600 Mg Miconazole Nitrate 3 Vag) was diagnosed with genital infection fungal and. Location: UNITED STATES , weighting 120.0 lb, Patient had the following side effects: abdominal distension, abdominal pain (What is abdominal pain?), constipation (What is constipation?), rash (What is rash?), skin ulcer, vaginal haemorrhage.

5095811-6 | Blood Bilirubin Increased, Blood Creatinine Increased, Blood Urea Increased, Haemoglobin Decreased, Neutrophil Percentage Decreased, Platelet Count Decreased, Red Blood Cell Count Decreased, White Blood Cell Count Decreased
on Aug 24, 2006 Male patient from JAPAN , 67 years of age, was diagnosed with gastrointestinal fungal infection and was treated with Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: blood bilirubin increased, blood creatinine increased, blood urea increased, haemoglobin decreased, neutrophil percentage decreased, platelet count decreased, red blood cell count decreased, white blood cell count decreased. Miconazole dosage: . During the same period patient was treated with CEFOTAXIME SODIUM (View Cefotaxime Sodium Review and Cefotaxime Sodium Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), METHYPHENIDATE HYDROCHLORIDE (View Methyphenidate Hydrochloride Review and Methyphenidate Hydrochloride Label ).

5061497-X | Haemorrhage Subcutaneous, Paralysis
on Jul 20, 2006 Female patient from JAPAN , 79 years of age, was diagnosed with oral candidiasis and was treated with Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: haemorrhage subcutaneous, paralysis (What is paralysis?). Miconazole dosage: . During the same period patient was treated with ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), TEPRENONE (View Teprenone Review and Teprenone Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), DILTIAZEM HYDROCHLORIDE (View Diltiazem Hydrochloride Review and Diltiazem Hydrochloride Label ).

5021885-4 | Haemorrhage Subcutaneous, Paralysis
Patient was taking Miconazole (View Usage). Patient had the following side effects: haemorrhage subcutaneous, paralysis (What is paralysis?) on Mar 16, 2006 from JAPAN Additional patient health information: Female patient , 79 years of age, was diagnosed with oral candidiasis and. Miconazole dosage: . During the same period patient was treated with ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), TEPRENONE (View Teprenone Review and Teprenone Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), DILTIAZEM HYDROCHLORIDE (View Diltiazem Hydrochloride Review and Diltiazem Hydrochloride Label ).

4980966-1 | Haematoma, Haemorrhage Subcutaneous, Illusion, International Normalised Ratio Increased, Monoplegia, Mouth Haemorrhage, Retroperitoneal Haemorrhage
Adverse event was reported on Apr 18, 2006 by a Male patient taking Miconazole (View Usage) (Dosage: ) was diagnosed with atrial fibrillation (What is atrial fibrillation?), hypertension, hyperuricaemia, constipation (What is constipation?) and. Location: JAPAN , weighting 164.5 lb, After Miconazole was administered, patient had the following side effects: haematoma, haemorrhage subcutaneous, illusion, international normalised ratio increased, monoplegia, mouth haemorrhage, retroperitoneal haemorrhage. During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ISOSORBIDE DINITRATE (View Isosorbide Dinitrate Review and Isosorbide Dinitrate Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), PROPRANOLOL HYDROCHLORIDE (View Propranolol Hydrochloride Review and Propranolol Hydrochloride Label ), METILDIGOXIN (View Metildigoxin Review and Metildigoxin Label ), MAGNESIUM OXIDE (View Magnesium Oxide Review and Magnesium Oxide Label ), NORTRIPTYLINE HCL (View Nortriptyline Hcl Review and Nortriptyline Hcl Label ). Patient was hospitalized.

4972128-9 | Haemorrhage Subcutaneous, Illusion, Paralysis, Retroperitoneal Haemorrhage
on Apr 04, 2006 Male patient from JAPAN , 74 years of age, was diagnosed with unevaluable event and was treated with Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: haemorrhage subcutaneous, illusion, paralysis (What is paralysis?), retroperitoneal haemorrhage. Miconazole dosage: . During the same period patient was treated with WARFARIN (View Warfarin Review and Warfarin Label ).

4959340-X | Injection Site Haemorrhage, International Normalised Ratio Increased, Small Intestinal Haemorrhage, Syncope
on Mar 22, 2006 Female patient from JAPAN , 59 years of age, was treated with Miconazole (View Usage). Patient had the following side effects: injection site haemorrhage, international normalised ratio increased, small intestinal haemorrhage, syncope. Miconazole dosage: . During the same period patient was treated with WARFARIN (View Warfarin Review and Warfarin Label ). Patient was hospitalized.

4948829-5 | International Normalised Ratio Increased, Small Intestinal Haemorrhage
Patient was taking Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: international normalised ratio increased, small intestinal haemorrhage on Mar 10, 2006 from JAPAN Additional patient health information: Female patient , 59 years of age, . Miconazole dosage: . Patient was hospitalized.

4870671-4 | Contusion, International Normalised Ratio Increased
Adverse event was reported on Dec 23, 2005 by a Male patient taking Miconazole (View Usage) (Dosage: ) was diagnosed with oral infection and. Location: UNITED KINGDOM , 77 years of age, Patient experienced the following unwanted or unexpected effects: contusion, international normalised ratio increased. During the same period patient was treated with WARFARIN (View Warfarin Review and Warfarin Label ). Patient was hospitalized.

4847002-9 | Anaemia, Haemorrhage
on Nov 29, 2005 Female patient from JAPAN , 68 years of age, was treated with Miconazole (View Usage). Patient had the following side effects: anaemia, haemorrhage. Miconazole dosage: .

4822969-3 | Blood Creatine Phosphokinase Increased, Liver Function Test Abnormal, Rhabdomyolysis
on Oct 28, 2005 Female patient from BELGIUM , 56 years of age, was diagnosed with fungal infection (What is fungal infection?) and was treated with Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: blood creatine phosphokinase increased, liver function test abnormal, rhabdomyolysis. Miconazole dosage: . During the same period patient was treated with CIPROFIBRATE (View Ciprofibrate Review and Ciprofibrate Label ). Patient was hospitalized.

4725804-7 | Refusal Of Treatment By Patient, Vaginal Discharge, Vaginal Swelling, Vulvovaginal Discomfort
Patient was taking Miconazole (View Usage). Patient experienced the following unwanted or unexpected effects: refusal of treatment by patient, vaginal discharge, vaginal swelling, vulvovaginal discomfort on Jul 22, 2005 from UNITED STATES Additional patient health information: Female patient , 23 years of age, was diagnosed with vaginal discharge, vaginal swelling, vulvovaginal discomfort and. Miconazole dosage: . Patient was hospitalized.

4711603-9 | Chills, Dyspnoea
Adverse event was reported on Jun 27, 2005 by a Male patient taking Miconazole (View Usage) (Dosage: ) . Location: JAPAN , 41 years of age, Patient had the following side effects: chills, dyspnoea. During the same period patient was treated with NAFAMOSTAT MESILATE (View Nafamostat Mesilate Review and Nafamostat Mesilate Label ), CITICOLINE (View Citicoline Review and Citicoline Label ), CEFPIROME SULFATE (View Cefpirome Sulfate Review and Cefpirome Sulfate Label ).

4705367-2 | Vasculitis Cerebral
on May 19, 2005 Female patient from JAPAN , 40 years of age, was treated with Miconazole (View Usage). After Miconazole was administered, patient had the following side effects: vasculitis cerebral. Miconazole dosage: 2mg 9 Times A Day For 16 Days.