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Summary

FDA Adverse Reports: 2030. View All

Ketek FDA safety alerts: 2006 2007

Reported deaths: 123

Reported hospitalizations: 758

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Often additional risks of using a medication, such as Ketek, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Ketek users, Learn more about unwanted side effects & find ways to reduce them. Browse Ketek Adverse Reports reported to FDA and participate in Ketek discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Ketek. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Ketek Adverse Effect Reports (FDA)

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Showing 1-50 of 2030  Next Page  >

6907930-7 | Respiratory Failure
on Jul 23, 2010 Male patient from SOUTH AFRICA , 88 years of age, was diagnosed with bronchopneumonia, myasthenia gravis and was treated with Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: respiratory failure. Ketek dosage: . During the same period patient was treated with MESTINON (View Mestinon Review and Mestinon Label ), SLOW K (View Slow-k Review and Slow-k Label ), PREDNISONE (View Prednisone Review and Prednisone Label ). Patient was hospitalized.

6819459-5 | Stevens-johnson Syndrome
Patient was taking Ketek (View Usage). Patient had the following side effects: stevens-johnson syndrome on Jun 28, 2010 from SOUTH AFRICA Additional patient health information: Male patient , 30 years of age, . Ketek dosage: . During the same period patient was treated with SINUCON ^LU CHEM^ (View Sinucon ^lu-chem^ Review and Sinucon ^lu-chem^ Label ). Patient was hospitalized.

6814972-9 | Dyspnoea, Rash
Adverse event was reported on Jun 25, 2010 by a Female patient taking Ketek (View Usage) (Dosage: ) was diagnosed with sinusitis (What is sinusitis?) and. Location: FRANCE , 43 years of age, After Ketek was administered, patient had the following side effects: dyspnoea, rash (What is rash?). During the same period patient was treated with APRANAX (View Apranax Review and Apranax Label ), CARDENSIEL (View Cardensiel Review and Cardensiel Label ). Patient was hospitalized.

6746446-8 | Alanine Aminotransferase Increased, Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Hepatitis Cholestatic, Jaundice, Pruritus
on May 17, 2010 Female patient from FRANCE , 81 years of age, was diagnosed with bronchitis (What is bronchitis?), thrombosis prophylaxis and was treated with Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, hepatitis cholestatic, jaundice (What is jaundice?), pruritus. Ketek dosage: . During the same period patient was treated with PREVISCAN (View Previscan Review and Previscan Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), AZOPT (View Azopt Review and Azopt Label ), ALPHAGAN (View Alphagan Review and Alphagan Label ), XALATAN (View Xalatan Review and Xalatan Label ), SINGULAIR (View Singulair Review and Singulair Label ). Patient was hospitalized.


6676327-X | Cytolytic Hepatitis, Hypoglycaemic Coma
on Apr 06, 2010 Male patient from FRANCE , 70 years of age, was diagnosed with insulin-requiring type 2 diabetes mellitus and was treated with Ketek (View Usage). Patient had the following side effects: cytolytic hepatitis, hypoglycaemic coma. Ketek dosage: . During the same period patient was treated with COLCHIMAX (View Colchimax Review and Colchimax Label ), NOVOMIX (View Novomix Review and Novomix Label ). Patient was hospitalized.

6657407-1 | Asthenia, Dysaesthesia, Facial Palsy, Paraesthesia, Vision Blurred
Patient was taking Ketek (View Usage). After Ketek was administered, patient had the following side effects: asthenia, dysaesthesia, facial palsy, paraesthesia, vision blurred on Mar 25, 2010 from FRANCE Additional patient health information: Male patient , 42 years of age, . Ketek dosage: . During the same period patient was treated with OSELTAMIVIR PHOSPHATE (View Oseltamivir Phosphate Review and Oseltamivir Phosphate Label ).

6639806-7 | Jaundice, Liver Disorder
Adverse event was reported on Mar 03, 2010 by a Male patient taking Ketek (View Usage) (Dosage: ) was diagnosed with pyrexia and. Location: JAPAN , 26 years of age, Patient experienced the following unwanted or unexpected effects: jaundice (What is jaundice?), liver disorder. Patient was hospitalized.

6535461-5 | Asthenia, Dysaesthesia, Facial Palsy, Paraesthesia, Vision Blurred
on Jan 11, 2010 Male patient from FRANCE , 42 years of age, was treated with Ketek (View Usage). Patient had the following side effects: asthenia, dysaesthesia, facial palsy, paraesthesia, vision blurred. Ketek dosage: . During the same period patient was treated with OSELTAMIVIR (View Oseltamivir Review and Oseltamivir Label ).

6522039-2 | Hepatitis Toxic, Liver Function Test Abnormal, Nausea, Vertigo
on Nov 11, 2009 Female patient from TURKEY , 30 years of age, weighting 136.7 lb, was diagnosed with pain (What is pain?) and was treated with Ketek (View Usage). After Ketek was administered, patient had the following side effects: hepatitis toxic, liver function test abnormal, nausea (What is nausea?), vertigo. Ketek dosage: . During the same period patient was treated with VOLTAREN (View Voltaren Review and Voltaren Label ). Patient was hospitalized.

6419600-2 | Abdominal Pain Upper, Asthenia, Eye Haemorrhage, Fatigue, Hepatitis Toxic, Thrombocytopenia
Patient was taking Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, asthenia, eye haemorrhage, fatigue, hepatitis toxic, thrombocytopenia on Oct 19, 2009 from SOUTH AFRICA Additional patient health information: Female patient , 31 years of age, was diagnosed with sinusitis (What is sinusitis?) and. Ketek dosage: . During the same period patient was treated with AVELON (View Avelon Review and Avelon Label ), ROCEPHIN (View Rocephin Review and Rocephin Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ). Patient was hospitalized.

6416132-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Dysgeusia, Heart Rate Increased, Heart Rate Irregular, Hepatic Enzyme Increased, Iron Deficiency Anaemia, Nausea
Adverse event was reported on Oct 22, 2009 by a Female patient taking Ketek (View Usage) (Dosage: Dose: 800 Mg) was diagnosed with lyme disease, fungal infection (What is fungal infection?) and. Location: UNITED STATES , weighting 130.3 lb, Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood lactate dehydrogenase increased, dysgeusia, heart rate increased, heart rate irregular, hepatic enzyme increased, iron deficiency anaemia, nausea (What is nausea?). During the same period patient was treated with HOMEOPATIC PREPARATION (Dose: Unk) (View Homeopatic Preparation Review and Homeopatic Preparation Label ), IRON INFUSION (Dose: Unk) (View Iron Infusion Review and Iron Infusion Label ), FLAGYL (Dose: 500 Mg Bid 2 Week On/ 2 Weeks Off) (View Flagyl Review and Flagyl Label ), VIT B 12 (Dose: 1-2/week) (View Vit B 12 Review and Vit B 12 Label ), NYSTATIN (Dose: Unk) (View Nystatin Review and Nystatin Label ), VALIUM (Dose: 1 Mg Alternate Nights) (View Valium Review and Valium Label ), XANAX (Dose: 0.5 Mg Alternate Nightsd) (View Xanax Review and Xanax Label ).

6408607-7 | Abdominal Pain Upper, Asthenia, Eye Haemorrhage, Fatigue, Hepatitis Toxic, Thrombocytopenia
on Oct 19, 2009 Female patient from SOUTH AFRICA , 31 years of age, was diagnosed with sinusitis (What is sinusitis?) and was treated with Ketek (View Usage). After Ketek was administered, patient had the following side effects: abdominal pain upper, asthenia, eye haemorrhage, fatigue, hepatitis toxic, thrombocytopenia. Ketek dosage: . During the same period patient was treated with AVELON (View Avelon Review and Avelon Label ). Patient was hospitalized.

6378793-6 | Dyspnoea, Empyema, Hyperhidrosis, Pyrexia
on Sep 16, 2009 Male patient from KOREA, REPUBLIC OF , 51 years of age, weighting 160.9 lb, was treated with Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, empyema, hyperhidrosis, pyrexia. Ketek dosage: . Patient was hospitalized.

6368655-2 | Bronchitis, Cough, Myalgia
Patient was taking Ketek (View Usage). Patient had the following side effects: bronchitis (What is bronchitis?), cough, myalgia on Sep 11, 2009 from KOREA, REPUBLIC OF Additional patient health information: Female patient , 64 years of age, weighting 110.2 lb, . Ketek dosage: . During the same period patient was treated with MUTERIN (View Muterin Review and Muterin Label ), NIZATIDINE (View Nizatidine Review and Nizatidine Label ), RINOEBASTEL (Dose Quantity: 1) (View Rinoebastel Review and Rinoebastel Label ). Patient was hospitalized.

6313562-4 | Abdominal Pain, Anuria, Bile Duct Obstruction, Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Urea Increased, Bone Marrow Failure, Diarrhoea, Dyspnoea
Adverse event was reported on Aug 10, 2009 by a Female patient taking Ketek (View Usage) (Dosage: ) was diagnosed with depression (What is depression?), anxiety (What is anxiety?) and. Location: UNITED STATES , weighting 140.0 lb, After Ketek was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), anuria, bile duct obstruction, blood creatinine increased, blood lactate dehydrogenase increased, blood urea increased, bone marrow failure, diarrhoea, dyspnoea. During the same period patient was treated with RENAGEL /01459902/ (View Renagel /01459902/ Review and Renagel /01459902/ Label ), VENLAFAXINE HYDROCHLORIDE (View Venlafaxine Hydrochloride Review and Venlafaxine Hydrochloride Label ), SOMA (View Soma Review and Soma Label ), XANAX (View Xanax Review and Xanax Label ), FLUCONAZOLE (Dose: Unk) (View Fluconazole Review and Fluconazole Label ), DIFLUCAN (Dose: Unk) (View Diflucan Review and Diflucan Label ), ZYVOX (Dose: Unk) (View Zyvox Review and Zyvox Label ), ZOSYN (Dose: Unk) (View Zosyn Review and Zosyn Label ). Patient was hospitalized and became disabled.

6301814-3 | Chest Pain, Oesophagitis, Rash
on Jul 30, 2009 Female patient from , 70 years of age, was treated with Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), oesophagitis, rash (What is rash?). Ketek dosage: . During the same period patient was treated with LOPRESSOR (View Lopressor Review and Lopressor Label ).

6301813-1 | Dermatitis Bullous
on Jul 30, 2009 Female patient from , 57 years of age, was treated with Ketek (View Usage). Patient had the following side effects: dermatitis bullous. Ketek dosage: . During the same period patient was treated with FOSCAVIR (View Foscavir Review and Foscavir Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ). Patient was hospitalized.

6282591-1 | Eosinophilia, Hepatitis Acute, Liver Injury
Patient was taking Ketek (View Usage). After Ketek was administered, patient had the following side effects: eosinophilia, hepatitis acute, liver injury on Jul 22, 2009 from UNITED STATES Additional patient health information: Female patient , 54 years of age, . Ketek dosage: .

6282591-1 | Eosinophilia, Hepatitis Acute, Liver Injury
Adverse event was reported on Jul 22, 2009 by a Female patient taking Ketek (View Usage) (Dosage: ) . Location: UNITED STATES , 54 years of age, Patient experienced the following unwanted or unexpected effects: eosinophilia, hepatitis acute, liver injury.

6282530-3 | Dizziness, Fatigue, Hepatitis Toxic
on Jul 13, 2009 Male patient from TURKEY , 33 years of age, was diagnosed with sinusitis (What is sinusitis?) and was treated with Ketek (View Usage). Patient had the following side effects: dizziness (What is dizziness?), fatigue, hepatitis toxic. Ketek dosage: . Patient was hospitalized.

6255037-7 | Hallucination, Hallucination, Auditory, Hallucination, Visual
on Jun 26, 2009 Female patient from JAPAN , 58 years of age, weighting 110.2 lb, was diagnosed with bronchitis (What is bronchitis?) and was treated with Ketek (View Usage). After Ketek was administered, patient had the following side effects: hallucination, hallucination, auditory, hallucination, visual. Ketek dosage: . During the same period patient was treated with MUCOSOLVAN (View Mucosolvan Review and Mucosolvan Label ).

6249660-3 | Hallucination
Patient was taking Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: hallucination on Jun 25, 2009 from JAPAN Additional patient health information: Female patient , 58 years of age, was diagnosed with bronchitis (What is bronchitis?) and. Ketek dosage: .

6243473-4 | Hallucination
Adverse event was reported on Jun 17, 2009 by a Female patient taking Ketek (View Usage) (Dosage: ) was diagnosed with bronchitis (What is bronchitis?) and. Location: JAPAN , 58 years of age, Patient had the following side effects: hallucination.

6223234-2 | Ammonia Increased, Asthenia, Confusional State, Dysarthria, Hepatic Cirrhosis, Hepatic Steatosis, Hepatomegaly, Lethargy, Liver Function Test Abnormal
on May 12, 2009 Male patient from UNITED STATES , weighting 265.5 lb, was diagnosed with glossitis, acute sinusitis and was treated with Ketek (View Usage). After Ketek was administered, patient had the following side effects: ammonia increased, asthenia, confusional state, dysarthria, hepatic cirrhosis, hepatic steatosis, hepatomegaly, lethargy, liver function test abnormal. Ketek dosage: Dose: 400x2. During the same period patient was treated with ERYTHROMYCIN (Dose: 400 Mg/5cc Swish And Spit) (View Erythromycin Review and Erythromycin Label ), DECADRON (Dose: Unk) (View Decadron Review and Decadron Label ), BENADRYL (Dose: 25 Mg/5cc Swish And Spit Out) (View Benadryl Review and Benadryl Label ). Patient was hospitalized.

6218750-3 | Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Creatinine Increased, Cardio-respiratory Arrest, Hypokalaemia, Liver Function Test Abnormal, Nervous System Disorder, Pupil Fixed
on May 26, 2009 Female patient from UNITED STATES , weighting 122.0 lb, was diagnosed with bronchitis (What is bronchitis?), vomiting, anxiety (What is anxiety?) and was treated with Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood creatinine increased, cardio-respiratory arrest, hypokalaemia, liver function test abnormal, nervous system disorder, pupil fixed. Ketek dosage: Dose: Unk. During the same period patient was treated with ZITHROMAX (Dose: Unk) (View Zithromax Review and Zithromax Label ), LEXAPRO (Dose: Unk) (View Lexapro Review and Lexapro Label ), BUSPAR (Dose: Unk) (View Buspar Review and Buspar Label ), NAPROSYN (Dose: Unk) (View Naprosyn Review and Naprosyn Label ), BIRTH CONTROL PILLS (Dose: Unk) (View Birth Control Pills Review and Birth Control Pills Label ). Patient was hospitalized.

6216130-8 | Dizziness, Fatigue, Hepatitis Toxic, Nausea
Patient was taking Ketek (View Usage). Patient had the following side effects: dizziness (What is dizziness?), fatigue, hepatitis toxic, nausea (What is nausea?) on May 27, 2009 from TURKEY Additional patient health information: Female patient , 23 years of age, weighting 112.4 lb, was diagnosed with sinusitis (What is sinusitis?) and. Ketek dosage: . During the same period patient was treated with AMPISID /00000502/ (View Ampisid /00000502/ Review and Ampisid /00000502/ Label ), ARVELES (View Arveles Review and Arveles Label ), RINOGEST /00076302/ (View Rinogest /00076302/ Review and Rinogest /00076302/ Label ), MUCOPLUS (View Mucoplus Review and Mucoplus Label ), ILIADIN (View Iliadin Review and Iliadin Label ), SUDAFED 12 HOUR (View Sudafed 12 Hour Review and Sudafed 12 Hour Label ), NASACORT (View Nasacort Review and Nasacort Label ). Patient was hospitalized.

6206789-3 | Epilepsy
Adverse event was reported on May 19, 2009 by a Female patient taking Ketek (View Usage) (Dosage: ) was diagnosed with sinobronchitis and. Location: SOUTH AFRICA , 26 years of age, After Ketek was administered, patient had the following side effects: epilepsy (What is epilepsy?). During the same period patient was treated with PROSPAN /01017801/ (View Prospan /01017801/ Review and Prospan /01017801/ Label ).

6206788-1 | Dizziness, Fatigue, Hepatitis Toxic, Nausea
on May 18, 2009 Female patient from TURKEY , 23 years of age, weighting 112.4 lb, was diagnosed with sinusitis (What is sinusitis?) and was treated with Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), fatigue, hepatitis toxic, nausea (What is nausea?). Ketek dosage: . During the same period patient was treated with AMPISID (View Ampisid Review and Ampisid Label ), ARVELES (View Arveles Review and Arveles Label ), RINOGEST /00076302/ (View Rinogest /00076302/ Review and Rinogest /00076302/ Label ), MUCOPLUS (View Mucoplus Review and Mucoplus Label ), ILIADIN (View Iliadin Review and Iliadin Label ), SUDAFED 12 HOUR (View Sudafed 12 Hour Review and Sudafed 12 Hour Label ), NASACORT (View Nasacort Review and Nasacort Label ). Patient was hospitalized.

6204049-8 | Abdominal Distension, Abdominal Pain Upper, Anorexia, Asthenia, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Chromaturia, Dehydration, Diarrhoea
on May 19, 2009 Female patient from UNITED STATES , weighting 210.4 lb, was diagnosed with pneumonia (What is pneumonia?) and was treated with Ketek (View Usage). Patient had the following side effects: abdominal distension, abdominal pain upper, anorexia, asthenia, blood alkaline phosphatase increased, blood bilirubin increased, chromaturia, dehydration, diarrhoea. Ketek dosage: . During the same period patient was treated with OFLOXACIN (Dose: Unk) (View Ofloxacin Review and Ofloxacin Label ), TYLENOL (Dose: Unk) (View Tylenol Review and Tylenol Label ), OTC (Dose: Unk) (View Otc Review and Otc Label ), ROCEPHIN (View Rocephin Review and Rocephin Label ), LEVAQUIN (Dose: Unk) (View Levaquin Review and Levaquin Label ), FLAGYL (Dose: Unk) (View Flagyl Review and Flagyl Label ), ZOSYN (Dose: Unk) (View Zosyn Review and Zosyn Label ). Patient was hospitalized.

6204047-4 | Ammonia Increased, Asthenia, Confusional State, Dysarthria, Hepatic Cirrhosis, Hepatic Steatosis, Hepatomegaly, Lethargy, Liver Function Test Abnormal
Patient was taking Ketek (View Usage). After Ketek was administered, patient had the following side effects: ammonia increased, asthenia, confusional state, dysarthria, hepatic cirrhosis, hepatic steatosis, hepatomegaly, lethargy, liver function test abnormal on May 12, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 265.5 lb, was diagnosed with glossitis, hypertension and. Ketek dosage: Dose: 400x2. During the same period patient was treated with ERYTHROMYCIN (Dose: 400 Mg/5cc Swish And Spit) (View Erythromycin Review and Erythromycin Label ), DECADRON (Dose: Unk) (View Decadron Review and Decadron Label ), BENADRYL (Dose: 25 Mg/5cc Swish And Spit Out) (View Benadryl Review and Benadryl Label ), BC (Dose: Unk) (View Bc Review and Bc Label ), ANTIHYPERTENSIVES (Dose: Unk) (View Antihypertensives Review and Antihypertensives Label ), DIOVAN HCT (Dose: 160/25 One A Day) (View Diovan Hct Review and Diovan Hct Label ), RITALIN (View Ritalin Review and Ritalin Label ). Patient was hospitalized.

6202323-2 | Abdominal Pain, Abdominal Pain Upper, Acute Hepatic Failure, Amenorrhoea, Ammonia Increased, Antinuclear Antibody Positive, Ascites, Back Pain, Blood Glucose Increased
Adverse event was reported on May 12, 2009 by a Female patient taking Ketek (View Usage) (Dosage: Dose: 800 400 Mg 2 Tabs Daily For 5 Days) . Location: UNITED STATES , weighting 154.0 lb, Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), abdominal pain upper, acute hepatic failure, amenorrhoea, ammonia increased, antinuclear antibody positive, ascites, back pain (What is back pain?), blood glucose increased. During the same period patient was treated with HERBAL PREPARATION (Dose: Unk) (View Herbal Preparation Review and Herbal Preparation Label ), NUTRITIONAL SUPPLEMENT (Dose: Unk) (View Nutritional Supplement Review and Nutritional Supplement Label ), GUAIFENESIN W/DEXTROMETHOR.HBR/PSEUDOEPHEDR. (Dose: Unk) (View Guaifenesin W/dextromethor.hbr/pseudoephedr. Review and Guaifenesin W/dextromethor.hbr/pseudoephedr. Label ), ALLERGY SHOTS (Dose: Unk) (View Allergy Shots Review and Allergy Shots Label ), ACIPHEX (Dose: Unk) (View Aciphex Review and Aciphex Label ), ALLEGRA (Dose: Unk) (View Allegra Review and Allegra Label ). Patient was hospitalized.

6202322-0 | Abdominal Pain Lower, Alanine Aminotransferase Increased, Antinuclear Antibody Positive, Arthralgia, Aspartate Aminotransferase Increased, Asthenia, Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased
on May 12, 2009 Female patient from UNITED STATES , weighting 145.1 lb, was diagnosed with upper respiratory tract infection and was treated with Ketek (View Usage). Patient had the following side effects: abdominal pain lower, alanine aminotransferase increased, antinuclear antibody positive, arthralgia, aspartate aminotransferase increased, asthenia, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased. Ketek dosage: . During the same period patient was treated with VITAMIN E (Dose: Unk) (View Vitamin E Review and Vitamin E Label ), FEMHRT (Dose: Unk) (View Femhrt Review and Femhrt Label ), ALLEGRA (Dose: Unk) (View Allegra Review and Allegra Label ), MULTI VITAMINS (Dose: Unk) (View Multi-vitamins Review and Multi-vitamins Label ), AMBI (Dose: Unk) (View Ambi Review and Ambi Label ), COUGHTUSS LIQUID (Dose: Unk) (View Coughtuss Liquid Review and Coughtuss Liquid Label ). Patient was hospitalized.

6202320-7 | Abdominal Pain, Abdominal Pain Upper, Decreased Appetite, Diarrhoea, Liver Function Test Abnormal, Mesenteric Vein Thrombosis, Nausea, Occult Blood Positive, Varicose Vein
on May 12, 2009 Male patient from UNITED STATES , weighting 286.6 lb, was treated with Ketek (View Usage). After Ketek was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), abdominal pain upper, decreased appetite, diarrhoea, liver function test abnormal, mesenteric vein thrombosis, nausea (What is nausea?), occult blood positive, varicose vein (What is varicose vein?). Ketek dosage: . During the same period patient was treated with RHINOCORT (Dose: Unk) (View Rhinocort Review and Rhinocort Label ), SINGULAIR (View Singulair Review and Singulair Label ), NEXIUM (Dose: Unk) (View Nexium Review and Nexium Label ), ALLEGRA (View Allegra Review and Allegra Label ). Patient was hospitalized.

6199507-9 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Hypertransaminasaemia, Nausea
Patient was taking Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, hypertransaminasaemia, nausea (What is nausea?) on May 12, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 165.0 lb, was diagnosed with acute sinusitis, sinus congestion, hypothyroidism and. Ketek dosage: . During the same period patient was treated with AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label ), ALLEGRA D 12 HOUR (Dose: 1 Tab) (View Allegra-d 12 Hour Review and Allegra-d 12 Hour Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), ESTROGENIC SUBSTANCE (Dose: Unk) (View Estrogenic Substance Review and Estrogenic Substance Label ), ASTELIN /00884002/ (Dose: Unk) (View Astelin /00884002/ Review and Astelin /00884002/ Label ), DARVOCET N 100 (Dose: Unk) (View Darvocet-n 100 Review and Darvocet-n 100 Label ), LEVAQUIN (Dose: Unk) (View Levaquin Review and Levaquin Label ), MEDROL (View Medrol Review and Medrol Label ). Patient was hospitalized.

6199506-7 | Anorexia, Blood Albumin Decreased, Blood Bilirubin Increased, Chills, Cholestatic Liver Injury, Fatigue, Haematuria, Herpes Zoster, Jaundice
Adverse event was reported on May 12, 2009 by a Female patient taking Ketek (View Usage) (Dosage: ) was diagnosed with chronic sinusitis, osteopenia and. Location: UNITED STATES , weighting 109.1 lb, Patient had the following side effects: anorexia, blood albumin decreased, blood bilirubin increased, chills, cholestatic liver injury, fatigue, haematuria, herpes zoster, jaundice (What is jaundice?). During the same period patient was treated with PREDNISONE (View Prednisone Review and Prednisone Label ), MOTRIN (View Motrin Review and Motrin Label ), AUGMENTIN '125' (Dose: Unk) (View Augmentin '125' Review and Augmentin '125' Label ), ZITHROMAX (Dose: Unk) (View Zithromax Review and Zithromax Label ), ZOCOR (View Zocor Review and Zocor Label ), HERBAL PREPARATION (Dose: Unk) (View Herbal Preparation Review and Herbal Preparation Label ), FOSAMAX (Dose: Unk) (View Fosamax Review and Fosamax Label ).

6199505-5 | Alanine Aminotransferase Increased, Anaemia, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Eosinophilia, Hepatic Enzyme Increased, Hyponatraemia, Lymphocytosis, Marrow Hyperplasia
on May 12, 2009 Male patient from UNITED STATES , weighting 164.3 lb, was treated with Ketek (View Usage). After Ketek was administered, patient had the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, blood alkaline phosphatase increased, eosinophilia, hepatic enzyme increased, hyponatraemia, lymphocytosis, marrow hyperplasia. Ketek dosage: Dose: Unk. During the same period patient was treated with AVELOX (Dose: Unk) (View Avelox Review and Avelox Label ), LOTREL (Dose: 5/20) (View Lotrel Review and Lotrel Label ), BENAZEPRIL HYDROCHLORIDE (View Benazepril Hydrochloride Review and Benazepril Hydrochloride Label ), LIPITOR (View Lipitor Review and Lipitor Label ), ASPIRIN (Dose: 81 (2 Tabs)) (View Aspirin Review and Aspirin Label ), LEVAQUIN (View Levaquin Review and Levaquin Label ). Patient was hospitalized.

6199504-3 | Abdominal Distension, Abdominal Pain Upper, Acute Hepatic Failure, Acute Respiratory Failure, Alanine Aminotransferase Increased, Ascites, Aspartate Aminotransferase Increased, Azotaemia, Blood Bilirubin Increased
on May 12, 2009 Male patient from UNITED STATES , weighting 220.5 lb, was diagnosed with bronchitis (What is bronchitis?), pneumonia (What is pneumonia?) and was treated with Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal distension, abdominal pain upper, acute hepatic failure, acute respiratory failure, alanine aminotransferase increased, ascites, aspartate aminotransferase increased, azotaemia, blood bilirubin increased. Ketek dosage: Dose: 1 Tab. During the same period patient was treated with PAXIL (Dose: Unk) (View Paxil Review and Paxil Label ), PREDNISONE (Dose: Unk) (View Prednisone Review and Prednisone Label ), ANTIBIOTICS (View Antibiotics Review and Antibiotics Label ). Patient was hospitalized.

6199503-1 | Alanine Aminotransferase Increased, Arthralgia, Aspartate Aminotransferase Increased, Biliary Cirrhosis Primary, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Fatigue, Hyperglycaemia, Jaundice
Patient was taking Ketek (View Usage). Patient had the following side effects: alanine aminotransferase increased, arthralgia, aspartate aminotransferase increased, biliary cirrhosis primary, blood alkaline phosphatase increased, blood bilirubin increased, fatigue, hyperglycaemia, jaundice (What is jaundice?) on May 12, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 164.0 lb, . Ketek dosage: .

6199502-X | Abnormal Sensation In Eye, Asthenia, Chills, Fatigue, Headache, Hepatic Enzyme Increased, Hepatitis, Hyperhidrosis, Malaise
Adverse event was reported on May 12, 2009 by a Male patient taking Ketek (View Usage) (Dosage: Dose: Unk) . Location: UNITED STATES , weighting 195.3 lb, After Ketek was administered, patient had the following side effects: abnormal sensation in eye, asthenia, chills, fatigue, headache (What is headache?), hepatic enzyme increased, hepatitis (What is hepatitis?), hyperhidrosis, malaise. During the same period patient was treated with ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ). Patient was hospitalized.

6199501-8 | Acute Myocardial Infarction, Blood Bilirubin Increased, Cardiogenic Shock, Hepatitis Acute, Liver Function Test Abnormal
on May 12, 2009 Male patient from UNITED STATES , weighting 230.5 lb, was treated with Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: acute myocardial infarction, blood bilirubin increased, cardiogenic shock, hepatitis acute, liver function test abnormal. Ketek dosage: Dose: Unk. During the same period patient was treated with ROCEPHIN (View Rocephin Review and Rocephin Label ), BIAXIN XL (Dose: 2 Tabs For 10 Days) (View Biaxin Xl Review and Biaxin Xl Label ), MEDROL (Dose: Unk) (View Medrol Review and Medrol Label ), ATUSS MR (Dose: 1-2 Teaspoon Every 4-6 Hours) (View Atuss Mr Review and Atuss Mr Label ), DEPO MEDROL (View Depo-medrol Review and Depo-medrol Label ).

6199500-6 | Ageusia, Ammonia Increased, Aphonia, Asthenia, Chromaturia, Coagulopathy, Dysphagia, Fatigue, Glossodynia
on May 12, 2009 Female patient from UNITED STATES , weighting 155.3 lb, was diagnosed with chronic sinusitis and was treated with Ketek (View Usage). Patient had the following side effects: ageusia, ammonia increased, aphonia, asthenia, chromaturia, coagulopathy, dysphagia, fatigue, glossodynia. Ketek dosage: . During the same period patient was treated with MINOCYCLINE HCL (Dose: Unk) (View Minocycline Hcl Review and Minocycline Hcl Label ), AZITHROMYCIN (Dose: Severval Prescriptions) (View Azithromycin Review and Azithromycin Label ), LIPITOR (View Lipitor Review and Lipitor Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ), ATROVENT (View Atrovent Review and Atrovent Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), PREMARIN (View Premarin Review and Premarin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6199499-2 | Abdominal Discomfort, Abdominal Distension, Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Change Of Bowel Habit, Cholecystitis, Cholelithiasis, Dizziness
Patient was taking Ketek (View Usage). After Ketek was administered, patient had the following side effects: abdominal discomfort, abdominal distension, abdominal pain (What is abdominal pain?), alanine aminotransferase increased, aspartate aminotransferase increased, change of bowel habit, cholecystitis, cholelithiasis, dizziness (What is dizziness?) on May 12, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 241.5 lb, was diagnosed with upper respiratory tract infection and. Ketek dosage: Dose: Unk. During the same period patient was treated with ATUSS DM (Dose: Unk) (View Atuss Dm Review and Atuss Dm Label ), PHENERGAN GEL (Dose: Unk) (View Phenergan Gel Review and Phenergan Gel Label ), MYLANTA /00036701/ (Dose: Unk) (View Mylanta /00036701/ Review and Mylanta /00036701/ Label ), TYLENOL (Dose: Unk) (View Tylenol Review and Tylenol Label ), MOTRIN (Dose: Unk) (View Motrin Review and Motrin Label ), DOXYCYCLINE (Dose: Unk) (View Doxycycline Review and Doxycycline Label ), ANTIBIOTICS (Dose: Unk) (View Antibiotics Review and Antibiotics Label ). Patient was hospitalized.

6198246-8 | Aspartate Aminotransferase Increased, Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Chromaturia, Hepatitis, Jaundice, Lipase Abnormal, Nausea
Adverse event was reported on May 12, 2009 by a Female patient taking Ketek (View Usage) (Dosage: Dose: 2 Tablets) was diagnosed with nausea (What is nausea?), sinusitis (What is sinusitis?), bronchitis (What is bronchitis?) and. Location: , weighting 180.0 lb, Patient experienced the following unwanted or unexpected effects: aspartate aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, chromaturia, hepatitis (What is hepatitis?), jaundice (What is jaundice?), lipase abnormal, nausea (What is nausea?). During the same period patient was treated with ZITHROMAX (Dose: Unk) (View Zithromax Review and Zithromax Label ), ALLEGRA (Dose: Unk) (View Allegra Review and Allegra Label ), ESTRATEST (Dose: Unk) (View Estratest Review and Estratest Label ), IBUPROFEN (Dose: Unk) (View Ibuprofen Review and Ibuprofen Label ), ALLERGY INJECTIONS (Dose: Unk) (View Allergy Injections Review and Allergy Injections Label ), PHENERGAN (View Phenergan Review and Phenergan Label ), LEVAQUIN (Dose: Unk) (View Levaquin Review and Levaquin Label ).

6198245-6 | Abdominal Pain Upper, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Chromaturia, Eye Movement Disorder, Fatigue, Hepatitis Acute, Malaise
on May 12, 2009 Female patient from UNITED STATES , weighting 160.3 lb, was diagnosed with bronchitis (What is bronchitis?) and was treated with Ketek (View Usage). Patient had the following side effects: abdominal pain upper, alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, chromaturia, eye movement disorder, fatigue, hepatitis acute, malaise. Ketek dosage: . During the same period patient was treated with FLEXERIL (Dose: Unk) (View Flexeril Review and Flexeril Label ), LEVAQUIN (Dose: Unk) (View Levaquin Review and Levaquin Label ), CYCLOBENZAPRINE (Dose: Unk) (View Cyclobenzaprine Review and Cyclobenzaprine Label ), NAPROSYN (Dose: Unk) (View Naprosyn Review and Naprosyn Label ), OPIUM ALKALOIDS AND DERIVATIVES (Dose: Unk) (View Opium Alkaloids And Derivatives Review and Opium Alkaloids And Derivatives Label ), KEFLEX (Dose: Unk) (View Keflex Review and Keflex Label ), AZITHROMYCIN (Dose: Unk) (View Azithromycin Review and Azithromycin Label ), AMOXICILLIN (Dose: Unk) (View Amoxicillin Review and Amoxicillin Label ). Patient was hospitalized.

6198244-4 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Chest Pain, Cold Sweat, Dyspnoea, Electrocardiogram St Segment Depression, Gamma-glutamyltransferase Increased, Hepatitis Fulminant
on May 12, 2009 Female patient from UNITED STATES , weighting 130.0 lb, was treated with Ketek (View Usage). After Ketek was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, chest pain (What is chest pain?), cold sweat, dyspnoea, electrocardiogram st segment depression, gamma-glutamyltransferase increased, hepatitis fulminant. Ketek dosage: Dose: Unk. During the same period patient was treated with VALTREX (Dose: Unk) (View Valtrex Review and Valtrex Label ), ROCEPHIN (Dose: Unk) (View Rocephin Review and Rocephin Label ), XANAX (Dose: Unk) (View Xanax Review and Xanax Label ), LEXAPRO (Dose: Unk) (View Lexapro Review and Lexapro Label ), VIT D (Dose: Unk) (View Vit D Review and Vit D Label ), CENTRUM SILVER /01292501/ (Dose: Unk) (View Centrum Silver /01292501/ Review and Centrum Silver /01292501/ Label ), CALCIUM (Dose: Unk) (View Calcium Review and Calcium Label ), LIQUIFED (Dose: Unk) (View Liquifed Review and Liquifed Label ). Patient was hospitalized.

6198243-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Constipation, Hepatitis Toxic, International Normalised Ratio Abnormal, Prothrombin Time Prolonged
Patient was taking Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, constipation (What is constipation?), hepatitis toxic, international normalised ratio abnormal, prothrombin time prolonged on May 12, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 223.0 lb, . Ketek dosage: Dose: Unk. During the same period patient was treated with DIOVAN HCT (View Diovan Hct Review and Diovan Hct Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FISH OIL (Dose: Unk) (View Fish Oil Review and Fish Oil Label ), COUMADIN (Dose: Unk) (View Coumadin Review and Coumadin Label ).

6198240-7 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Eosinophil Count Increased, Liver Function Test Abnormal
Adverse event was reported on May 12, 2009 by a Female patient taking Ketek (View Usage) (Dosage: Dose: Unk) was diagnosed with sinusitis (What is sinusitis?) and. Location: UNITED STATES , 48 years of age, Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood lactate dehydrogenase increased, eosinophil count increased, liver function test abnormal.

6196217-9 | Cough, Diarrhoea, Dysgeusia, Dyspnoea, Fatigue, Headache, Hepatitis, Hyperhidrosis, Hypoaesthesia
on May 12, 2009 Male patient from UNITED STATES , weighting 185.0 lb, was diagnosed with pneumonia (What is pneumonia?) and was treated with Ketek (View Usage). After Ketek was administered, patient had the following side effects: cough, diarrhoea, dysgeusia, dyspnoea, fatigue, headache (What is headache?), hepatitis (What is hepatitis?), hyperhidrosis, hypoaesthesia. Ketek dosage: . During the same period patient was treated with ASPIRIN (Dose: Unk) (View Aspirin Review and Aspirin Label ), IBUPROFEN (Dose: Unk) (View Ibuprofen Review and Ibuprofen Label ), LEVAQUIN (View Levaquin Review and Levaquin Label ).

6196216-7 | Abdominal Pain Upper, Asthenia, Chills, Chromaturia, Decreased Appetite, Flank Pain, Headache, Hepatitis, Liver Function Test Abnormal
on May 12, 2009 Male patient from UNITED STATES , weighting 182.4 lb, was diagnosed with chronic sinusitis and was treated with Ketek (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, asthenia, chills, chromaturia, decreased appetite, flank pain, headache (What is headache?), hepatitis (What is hepatitis?), liver function test abnormal. Ketek dosage: . During the same period patient was treated with BACTRIM (Dose: Unk) (View Bactrim Review and Bactrim Label ), BIAXIN (Dose: Unk) (View Biaxin Review and Biaxin Label ), MEDROL (Dose: Unk) (View Medrol Review and Medrol Label ), ZITHROMAX (Dose: Unk) (View Zithromax Review and Zithromax Label ), ACIPHEX (Dose: Unk) (View Aciphex Review and Aciphex Label ), LIPITOR (Dose: Unk) (View Lipitor Review and Lipitor Label ).

6196215-5 | Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Cardiomegaly, Chest Pain, Diarrhoea, Hepatitis Viral, Liver Function Test Abnormal, Nausea
Patient was taking Ketek (View Usage). Patient had the following side effects: blood alkaline phosphatase increased, blood bilirubin increased, cardiomegaly, chest pain (What is chest pain?), diarrhoea, hepatitis viral, liver function test abnormal, nausea (What is nausea?) on May 12, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 151.9 lb, . Ketek dosage: Dose: Unk. During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), ACIPHEX (View Aciphex Review and Aciphex Label ), VITAMINS NOS (Dose: Unk) (View Vitamins Nos Review and Vitamins Nos Label ), CLIMARA PRO (Dose: Unk) (View Climara Pro Review and Climara Pro Label ), ALCOHOL (Dose: Unk) (View Alcohol Review and Alcohol Label ).

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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Ketek risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Ketek quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Ketek use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Ketek Reactions
Abdominal Distension
Abdominal PainWhat is Abdominal pain?
Abdominal Pain Upper
Alanine Aminotransferase Increased
Anorexia
Ascites
Aspartate Aminotransferase Increased
Asthenia
Bilirubin Conjugated Increased
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Chest PainWhat is Chest pain?
Chills
Chromaturia
Diarrhoea
Diplopia
DizzinessWhat is Dizziness?
Dyspnoea
Fatigue
HeadacheWhat is Headache?
Hepatic Enzyme Increased
HepatitisWhat is Hepatitis?
JaundiceWhat is Jaundice?
Liver Function Test Abnormal
Loss Of Consciousness
NauseaWhat is Nausea?
Pyrexia
Vision Blurred
Visual Disturbance
Vomiting
Ketek Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Ketek adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!