AUGMENTIN Side Effects

6964062-X | Abdominal Pain, Blood Potassium Decreased, Clostridial Infection, Dehydration, Diarrhoea, Hypotension
on Sep 02, 2010 Female patient from UNITED STATES , 64 years of age, weighting 120.0 lb, was diagnosed with ear disorder, sinus headache and was treated with Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), blood potassium decreased, clostridial infection, dehydration, diarrhoea, hypotension. Augmentin dosage: 1/2 Tab Twice Day 047. Patient was hospitalized.

6741073-0 | Headache, Movement Disorder, Musculoskeletal Stiffness, No Therapeutic Response, Pain
Patient was taking Augmentin (View Usage). Patient had the following side effects: headache (What is headache?), movement disorder (What is movement disorder?), musculoskeletal stiffness, no therapeutic response, pain (What is pain?) on May 25, 2010 from UNITED STATES Additional patient health information: Female patient , 54 years of age, weighting 209.0 lb, was diagnosed with oropharyngeal pain and. Augmentin dosage: 14 Tablets Twic Daily Po.

6712826-X | Rash Pustular
Adverse event was reported on May 28, 2009 by a Female patient taking Augmentin (View Usage) (Dosage: 1tsp Three Times Per Day) . Location: UNITED STATES , child 10 years of age, After Augmentin was administered, patient had the following side effects: rash pustular. During the same period patient was treated with BACTROBAN (View Bactroban Review and Bactroban Label ).

6712803-9 | Clostridium Difficile Colitis
on Jul 06, 2009 Female patient from UNITED STATES , 64 years of age, was diagnosed with pneumonia (What is pneumonia?), multiple sclerosis (What is multiple sclerosis?) and was treated with Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: clostridium difficile colitis. Augmentin dosage: . During the same period patient was treated with BETASERON (8mu Alternate Days) (View Betaseron Review and Betaseron Label ). Patient was hospitalized.


6712801-5 | Hypersensitivity
on Jun 18, 2009 Female patient from UNITED STATES , 84 years of age, was treated with Augmentin (View Usage). Patient had the following side effects: hypersensitivity. Augmentin dosage: .

6712800-3 | Clostridium Difficile Colitis
Patient was taking Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: clostridium difficile colitis on Jul 07, 2009 from UNITED STATES Additional patient health information: Female patient , 64 years of age, was diagnosed with pneumonia (What is pneumonia?), multiple sclerosis (What is multiple sclerosis?) and. Augmentin dosage: . During the same period patient was treated with BETASERON (View Betaseron Review and Betaseron Label ). Patient was hospitalized.

6712799-X | Fungal Infection
Adverse event was reported on May 12, 2009 by a Female patient taking Augmentin (View Usage) (Dosage: ) . Location: UNITED STATES , 56 years of age, Patient experienced the following unwanted or unexpected effects: fungal infection (What is fungal infection?).

6656092-2 | Blood Creatinine Increased, Diarrhoea, Electrolyte Imbalance, Hyperbilirubinaemia, Hypoglycaemia, Jaundice, Liver Function Test Abnormal
on Mar 23, 2010 Female patient from GREECE , 77 years of age, was diagnosed with urinary tract infection (What is urinary tract infection?) and was treated with Augmentin (View Usage). Patient had the following side effects: blood creatinine increased, diarrhoea, electrolyte imbalance, hyperbilirubinaemia, hypoglycaemia, jaundice (What is jaundice?), liver function test abnormal. Augmentin dosage: . During the same period patient was treated with SOLOSA (View Solosa Review and Solosa Label ). Patient was hospitalized.

6653853-0 | Infectious Mononucleosis, Rash
on Mar 16, 2010 Female patient from RUSSIAN FEDERATION , child 2 years of age, was treated with Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: infectious mononucleosis (What is infectious mononucleosis?), rash (What is rash?). Augmentin dosage: . Patient was hospitalized.

6653847-5 | Atrophic Glossitis, Interstitial Lung Disease, Laryngeal Oedema, Prurigo, Rash Macular, Tongue Disorder
Patient was taking Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: atrophic glossitis, interstitial lung disease, laryngeal oedema, prurigo, rash macular, tongue disorder on Mar 24, 2010 from FRANCE Additional patient health information: Female patient , 78 years of age, was diagnosed with superinfection, atrial fibrillation (What is atrial fibrillation?) and. Augmentin dosage: . During the same period patient was treated with KARDEGIC (View Kardegic Review and Kardegic Label ), AMLOR (View Amlor Review and Amlor Label ), CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), RISPERDAL (View Risperdal Review and Risperdal Label ), CORDARONE (View Cordarone Review and Cordarone Label ). Patient was hospitalized.

6653409-X | Autoimmune Hepatitis, Cholelithiasis, Gallbladder Polyp, Hepatitis Cholestatic, Liver Injury, Staphylococcal Abscess
Adverse event was reported on Mar 17, 2010 by a Female patient taking Augmentin (View Usage) (Dosage: ) . Location: UNITED STATES , 33 years of age, Patient had the following side effects: autoimmune hepatitis, cholelithiasis, gallbladder polyp, hepatitis cholestatic, liver injury, staphylococcal abscess. During the same period patient was treated with BACTRIM (View Bactrim Review and Bactrim Label ).

6653391-5 | Hepatic Cirrhosis, Hepatic Steatosis, Hepatitis Alcoholic, Liver Injury, Phlebosclerosis, Rash
on Mar 17, 2010 Male patient from UNITED STATES , 77 years of age, was treated with Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: hepatic cirrhosis, hepatic steatosis, hepatitis alcoholic, liver injury, phlebosclerosis, rash (What is rash?). Augmentin dosage: . During the same period patient was treated with KEFLEX (View Keflex Review and Keflex Label ).

6651568-6 | Clonus, Grand Mal Convulsion, Hypoaesthesia
on Mar 22, 2010 Male patient from FRANCE , 35 years of age, was diagnosed with pyelonephritis, epilepsy (What is epilepsy?) and was treated with Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: clonus, grand mal convulsion, hypoaesthesia. Augmentin dosage: 1g Three Times Per Day. During the same period patient was treated with TEGRETOL (200mg Twice Per Day) (View Tegretol Review and Tegretol Label ). Patient was hospitalized.

6651557-1 | Anaphylactic Shock, Dermatitis Contact, Loss Of Consciousness, Rash, Vomiting
Patient was taking Augmentin (View Usage). Patient had the following side effects: anaphylactic shock, dermatitis contact, loss of consciousness, rash (What is rash?), vomiting on Mar 17, 2010 from LUXEMBOURG Additional patient health information: Male patient , weighting 187.4 lb, was diagnosed with bronchitis (What is bronchitis?) and. Augmentin dosage: 3tab Per Day. During the same period patient was treated with LYSOX (View Lysox Review and Lysox Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), DAFALGAN (View Dafalgan Review and Dafalgan Label ), NASENSPRAY RATIOPHARM (View Nasenspray Ratiopharm Review and Nasenspray Ratiopharm Label ). Patient was hospitalized.

6649207-3 | Asthenia, Body Temperature Decreased, Cold Sweat, Leukopenia, Monocytosis
Adverse event was reported on Mar 17, 2010 by a Female patient taking Augmentin (View Usage) (Dosage: 800mg Per Day) was diagnosed with acute tonsillitis and. Location: RUSSIAN FEDERATION , child 7 years of age, After Augmentin was administered, patient had the following side effects: asthenia, body temperature decreased, cold sweat, leukopenia, monocytosis. During the same period patient was treated with CETIRIZINE HCL (10drop Per Day) (View Cetirizine Hcl Review and Cetirizine Hcl Label ).

6643041-6 | Idiopathic Thrombocytopenic Purpura, Renal Failure Acute
on Mar 11, 2010 Male patient from SPAIN , 75 years of age, was diagnosed with upper respiratory tract infection and was treated with Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: idiopathic thrombocytopenic purpura, renal failure acute. Augmentin dosage: . During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), ADIRO (View Adiro Review and Adiro Label ), UNIKET (View Uniket Review and Uniket Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), OMNIC (View Omnic Review and Omnic Label ). Patient was hospitalized.

6641015-2 | Contraindication To Medical Treatment, Dermatitis Exfoliative, Pruritus
on Mar 15, 2010 Female patient from FRANCE , 78 years of age, was treated with Augmentin (View Usage). Patient had the following side effects: contraindication to medical treatment, dermatitis exfoliative, pruritus. Augmentin dosage: 1g Three Times Per Day. Patient was hospitalized.

6641013-9 | Abdominal Distension, Auricular Swelling, Chest Discomfort, Diarrhoea, Disbacteriosis, Dysphagia, Dyspnoea, Eyelid Oedema, Face Oedema
Patient was taking Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: abdominal distension, auricular swelling, chest discomfort, diarrhoea, disbacteriosis, dysphagia, dyspnoea, eyelid oedema, face oedema on Mar 12, 2010 from FRANCE Additional patient health information: Female patient , 54 years of age, was diagnosed with parotitis and. Augmentin dosage: . During the same period patient was treated with MICARDIS (View Micardis Review and Micardis Label ), ABUFENE (View Abufene Review and Abufene Label ), LINSEED OIL (View Linseed Oil Review and Linseed Oil Label ), SOLUPRED (View Solupred Review and Solupred Label ). Patient was hospitalized.

6640997-2 | Blood Creatinine Increased, Diarrhoea, Electrolyte Imbalance, Hyperbilirubinaemia, Hypoglycaemia, Jaundice
Adverse event was reported on Mar 08, 2010 by a Female patient taking Augmentin (View Usage) (Dosage: ) was diagnosed with urinary tract infection (What is urinary tract infection?) and. Location: GREECE , 77 years of age, Patient experienced the following unwanted or unexpected effects: blood creatinine increased, diarrhoea, electrolyte imbalance, hyperbilirubinaemia, hypoglycaemia, jaundice (What is jaundice?). During the same period patient was treated with SOLOSA (View Solosa Review and Solosa Label ). Patient was hospitalized.

6638411-6 | Asthenia, Coagulopathy, Encephalopathy, Fatigue, Hypotension, Jaundice, Malaise, Mental Status Changes
on Mar 16, 2010 Female patient from UNITED STATES , 45 years of age, weighting 319.7 lb, was diagnosed with upper respiratory tract infection and was treated with Augmentin (View Usage). Patient had the following side effects: asthenia, coagulopathy, encephalopathy, fatigue, hypotension, jaundice (What is jaundice?), malaise, mental status changes. Augmentin dosage: 1750 Mg Daily Oral 047. Patient was hospitalized.

6638393-7 | Cardiac Arrest
on Mar 08, 2010 Female patient from UNITED KINGDOM , 35 years of age, weighting 143.3 lb, was treated with Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: cardiac arrest (What is cardiac arrest?). Augmentin dosage: .

6635357-4 | Cholestasis
Patient was taking Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: cholestasis on Mar 11, 2010 from UNITED STATES Additional patient health information: Male patient , 41 years of age, weighting 244.0 lb, was diagnosed with sinusitis (What is sinusitis?) and. Augmentin dosage: Augmentin Po. Less Than 7 Days. Patient was hospitalized.

6632331-9 | Haematuria, Haemoptysis, Pancytopenia
Adverse event was reported on Mar 08, 2010 by a Male patient taking Augmentin (View Usage) (Dosage: ) was diagnosed with respiratory tract infection, hiv infection (What is hiv infection?), cerebral toxoplasmosis and. Location: FRANCE , 46 years of age, Patient had the following side effects: haematuria, haemoptysis, pancytopenia. During the same period patient was treated with LOPERAMIDE HCL (2tabd Per Day) (View Loperamide Hcl Review and Loperamide Hcl Label ), INTELENCE (View Intelence Review and Intelence Label ), KIVEXA (View Kivexa Review and Kivexa Label ), DALACINE (View Dalacine Review and Dalacine Label ), MALOCIDE (View Malocide Review and Malocide Label ), PENTACARINAT (View Pentacarinat Review and Pentacarinat Label ). Patient was hospitalized.

6630267-0 | Atrophic Glossitis, Cheilitis, Dermatitis Exfoliative, Eosinophil Count Increased, Face Oedema, Hyperthermia, Lymphadenopathy, Oedema Peripheral
on Mar 08, 2010 Male patient from FRANCE , 48 years of age, was treated with Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: atrophic glossitis, cheilitis, dermatitis exfoliative, eosinophil count increased, face oedema, hyperthermia, lymphadenopathy, oedema peripheral. Augmentin dosage: . During the same period patient was treated with FORTUM (View Fortum Review and Fortum Label ), CIPROFLOXACIN HCL (View Ciprofloxacin Hcl Review and Ciprofloxacin Hcl Label ), AMIKACIN (View Amikacin Review and Amikacin Label ), VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ), FLAGYL (View Flagyl Review and Flagyl Label ), TAZOCILLINE (View Tazocilline Review and Tazocilline Label ). Patient was hospitalized.

6626124-6 | Gout
on Mar 05, 2010 Male patient from FRANCE , 30 years of age, was treated with Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: gout (What is gout?). Augmentin dosage: .

6626054-X | Abasia, Activated Partial Thromboplastin Time Prolonged, Acute Respiratory Distress Syndrome, Anaemia, Bacteraemia, Blood Culture Positive, Blood Fibrinogen Increased, Catheter Site Haemorrhage, Culture Urine Positive
Patient was taking Augmentin (View Usage). Patient had the following side effects: abasia, activated partial thromboplastin time prolonged, acute respiratory distress syndrome, anaemia, bacteraemia, blood culture positive, blood fibrinogen increased, catheter site haemorrhage, culture urine positive on Mar 08, 2010 from UNITED STATES Additional patient health information: Female patient , 64 years of age, was diagnosed with cough, herpes zoster, blood cholesterol increased and. Augmentin dosage: . During the same period patient was treated with ACYCLOVIR (400mg Three Times Per Day) (View Acyclovir Review and Acyclovir Label ), KAPIDEX (60mg Per Day) (View Kapidex Review and Kapidex Label ), CEFUROXIME (View Cefuroxime Review and Cefuroxime Label ), DIPHENOXYLATE (View Diphenoxylate Review and Diphenoxylate Label ), HYDROXYZINE (View Hydroxyzine Review and Hydroxyzine Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), THYROID TAB (120mg Per Day) (View Thyroid Tab Review and Thyroid Tab Label ). Patient was hospitalized.

6621083-4 | Breast Mass, Breast Swelling, Condition Aggravated, Contusion, Discomfort, Dry Skin, Fatigue, Gynaecomastia, Headache
Adverse event was reported on Mar 01, 2010 by a Male patient taking Augmentin (View Usage) (Dosage: 1g Three Times Per Day) . Location: UNITED KINGDOM , 63 years of age, After Augmentin was administered, patient had the following side effects: breast mass, breast swelling, condition aggravated, contusion, discomfort, dry skin, fatigue, gynaecomastia, headache (What is headache?). During the same period patient was treated with CHLORHEXIDINE GLUCONATE (View Chlorhexidine Gluconate Review and Chlorhexidine Gluconate Label ), VITAMIN K2 (View Vitamin K2 Review and Vitamin K2 Label ), VITAMINS + MINERALS (View Vitamins + Minerals Review and Vitamins + Minerals Label ).

6610769-3 | Anaphylactic Shock, Dermatitis Contact, Loss Of Consciousness, Rash, Vomiting
on Feb 19, 2010 Male patient from LUXEMBOURG , weighting 187.4 lb, was diagnosed with bronchitis (What is bronchitis?) and was treated with Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock, dermatitis contact, loss of consciousness, rash (What is rash?), vomiting. Augmentin dosage: 3tab Per Day. During the same period patient was treated with LYSOX (View Lysox Review and Lysox Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), DAFALGAN (View Dafalgan Review and Dafalgan Label ), NASENSPRAY RATIOPHARM (View Nasenspray Ratiopharm Review and Nasenspray Ratiopharm Label ). Patient was hospitalized.

6602411-2 | Choluria, Hepatitis
on Feb 18, 2010 Male patient from SPAIN , 53 years of age, was diagnosed with tooth infection and was treated with Augmentin (View Usage). Patient had the following side effects: choluria, hepatitis (What is hepatitis?). Augmentin dosage: 875mg Three Times Per Day.

6600185-2 | Erythema Multiforme, Parotitis
Patient was taking Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: erythema multiforme, parotitis on Feb 16, 2010 from UNITED KINGDOM Additional patient health information: Female patient , 73 years of age, was diagnosed with parotitis, prophylaxis, hypertension, constipation (What is constipation?) and. Augmentin dosage: . During the same period patient was treated with INFLUENZA VACCINE (SPLIT VIRION, INACTIVATED) (View Influenza Vaccine (split Virion, Inactivated) Review and Influenza Vaccine (split Virion, Inactivated) Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), LACTULOSE (View Lactulose Review and Lactulose Label ), PSYLLIUM (View Psyllium Review and Psyllium Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), BENDROFLUMETHIAZIDE (View Bendroflumethiazide Review and Bendroflumethiazide Label ). Patient was hospitalized.

6597076-2 | Anaphylactic Shock
Adverse event was reported on Feb 15, 2010 by a Female patient taking Augmentin (View Usage) (Dosage: 875mg Per Day) was diagnosed with tooth infection and. Location: SPAIN , 38 years of age, weighting 143.3 lb, Patient experienced the following unwanted or unexpected effects: anaphylactic shock.

6597074-9 | Abdominal Discomfort, Dizziness, Dyspepsia, Headache, Pruritus, Rash, Skin Reaction
on Feb 15, 2010 Female patient from MACEDONIA, THE FORMER YUGOSLAV REPUBLIC OF , 30 years of age, was diagnosed with upper respiratory tract infection and was treated with Augmentin (View Usage). Patient had the following side effects: abdominal discomfort, dizziness (What is dizziness?), dyspepsia, headache (What is headache?), pruritus, rash (What is rash?), skin reaction. Augmentin dosage: 1g Twice Per Day.

6595870-5 | No Therapeutic Response, Pain In Extremity
on Feb 19, 2010 Female patient from UNITED STATES , weighting 172.0 lb, was diagnosed with urinary tract infection (What is urinary tract infection?) and was treated with Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: no therapeutic response, pain in extremity. Augmentin dosage: 875-125 Mg Tab One Tablet Every 12 Hrs Mouth.

6594427-X | Diarrhoea, Laryngeal Oedema, Pruritus, Rash
Patient was taking Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, laryngeal oedema, pruritus, rash (What is rash?) on Feb 16, 2010 from RUSSIAN FEDERATION Additional patient health information: Male patient , weighting 202.8 lb, . Augmentin dosage: 2g Per Day.

6590694-7 | Faeces Discoloured, Gastritis
Adverse event was reported on Feb 12, 2010 by a Male patient taking Augmentin (View Usage) (Dosage: 1g Twice Per Day) was diagnosed with pain (What is pain?) and. Location: TUNISIA , 40 years of age, Patient had the following side effects: faeces discoloured, gastritis.

6590687-X | Condition Aggravated, Face Oedema, Gastrointestinal Disorder, Pruritus, Rash Pustular, Skin Lesion
on Feb 15, 2010 Female patient from FRANCE , 50 years of age, was diagnosed with sinusitis (What is sinusitis?) and was treated with Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: condition aggravated, face oedema, gastrointestinal disorder, pruritus, rash pustular, skin lesion. Augmentin dosage: 3g Per Day. During the same period patient was treated with CEFPODOXIME PROXETIL (View Cefpodoxime Proxetil Review and Cefpodoxime Proxetil Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ), DERINOX (View Derinox Review and Derinox Label ), INIPOMP (View Inipomp Review and Inipomp Label ). Patient was hospitalized.

6583299-5 | Blood Creatinine Increased, Diarrhoea, Multi-organ Failure, Rash, Rash Pruritic, Sepsis, Stevens-johnson Syndrome, Superinfection, Toxic Epidermal Necrolysis
on Feb 09, 2010 Female patient from SWITZERLAND , weighting 154.3 lb, was diagnosed with skin infection and was treated with Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, diarrhoea, multi-organ failure, rash (What is rash?), rash pruritic, sepsis (What is sepsis?), stevens-johnson syndrome, superinfection, toxic epidermal necrolysis. Augmentin dosage: 1g Twice Per Day. During the same period patient was treated with CIPROXIN (1g Per Day) (View Ciproxin Review and Ciproxin Label ), AMOXICILLIN AND CLAVULANATE POTASSIUM (1g Twice Per Day) (View Amoxicillin And Clavulanate Potassium Review and Amoxicillin And Clavulanate Potassium Label ), SPIRONOLACTONE (150mg Per Day) (View Spironolactone Review and Spironolactone Label ), FERRUM HAUSMANN (100mg Per Day) (View Ferrum Hausmann Review and Ferrum Hausmann Label ), ELTROXIN (.05mg Per Day) (View Eltroxin Review and Eltroxin Label ), CONCOR PLUS (5mg Per Day) (View Concor Plus Review and Concor Plus Label ), MAGNESIUM DIASPORAL (300mg Per Day) (View Magnesium Diasporal Review and Magnesium Diasporal Label ), NOVALGIN (View Novalgin Review and Novalgin Label ). Patient was hospitalized.

6583285-5 | Condition Aggravated, Eosinophilic Cellulitis, Face Oedema, Genital Erythema, Hyperthermia, Lymphadenopathy, Mucous Membrane Disorder, Orthostatic Hypotension, Pharyngeal Erythema
Patient was taking Augmentin (View Usage). Patient had the following side effects: condition aggravated, eosinophilic cellulitis, face oedema, genital erythema, hyperthermia, lymphadenopathy, mucous membrane disorder, orthostatic hypotension, pharyngeal erythema on Feb 12, 2010 from FRANCE Additional patient health information: Male patient , 36 years of age, . Augmentin dosage: . During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), EFFERALGAN (View Efferalgan Review and Efferalgan Label ). Patient was hospitalized.

6581499-1 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Gamma-glutamyltransferase Increased, Hepatocellular Injury, Liver Function Test Abnormal
Adverse event was reported on Feb 11, 2010 by a Male patient taking Augmentin (View Usage) (Dosage: 1g Four Times Per Day) was diagnosed with osteitis and. Location: FRANCE , 65 years of age, After Augmentin was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, gamma-glutamyltransferase increased, hepatocellular injury, liver function test abnormal. During the same period patient was treated with GENTALLINE (220mg Per Day) (View Gentalline Review and Gentalline Label ), LOVENOX (View Lovenox Review and Lovenox Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), BACTRIM DS (2unit Twice Per Day) (View Bactrim Ds Review and Bactrim Ds Label ), FLAGYL (500mg Three Times Per Day) (View Flagyl Review and Flagyl Label ). Patient was hospitalized.

6581379-1 | Diarrhoea, Multi-organ Failure, Rash, Sepsis, Toxic Epidermal Necrolysis, Vomiting
on Feb 10, 2010 Female patient from SWITZERLAND , 63 years of age, weighting 154.3 lb, was diagnosed with skin infection and was treated with Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, multi-organ failure, rash (What is rash?), sepsis (What is sepsis?), toxic epidermal necrolysis, vomiting. Augmentin dosage: Total Daily Dose: 2 G. During the same period patient was treated with CIPROXIN (Total Daily Dose: 1 G) (View Ciproxin Review and Ciproxin Label ), CO AMOXI MEPHA (Total Daily Dose: 2 G) (View Co-amoxi Mepha Review and Co-amoxi Mepha Label ), XENALON (Total Daily Dose: 150 Mg) (View Xenalon Review and Xenalon Label ), FERRUM HAUSMANN (Total Daily Dose: 100 Mg) (View Ferrum Hausmann Review and Ferrum Hausmann Label ), ELTROXIN (Total Daily Dose: 0.05 Mg) (View Eltroxin Review and Eltroxin Label ), CONCOR PLUS (As Used: 5/12.5 Mg) (View Concor Plus Review and Concor Plus Label ), MAGNESIUM DIASPORAL (Total Daily Dose: 300 Mg) (View Magnesium Diasporal Review and Magnesium Diasporal Label ), NOVALGIN (View Novalgin Review and Novalgin Label ). Patient was hospitalized.

6578302-2 | Dizziness, Paraesthesia, Vision Blurred
on Feb 04, 2010 Male patient from SPAIN , 54 years of age, weighting 187.4 lb, was treated with Augmentin (View Usage). Patient had the following side effects: dizziness (What is dizziness?), paraesthesia, vision blurred. Augmentin dosage: 2tab Twice Per Day. During the same period patient was treated with MERIEUX INACTIVATED RABIES VACCINE (View Merieux Inactivated Rabies Vaccine Review and Merieux Inactivated Rabies Vaccine Label ), IMMUNE GLOBULIN NOS (View Immune Globulin Nos Review and Immune Globulin Nos Label ).

6572177-3 | Erythema Multiforme, Pyrexia, Skin Lesion
Patient was taking Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: erythema multiforme, pyrexia, skin lesion on Feb 02, 2010 from FRANCE Additional patient health information: Male patient , child 3 years of age, . Augmentin dosage: .

6572175-X | Jaundice, Mixed Liver Injury
Adverse event was reported on Jan 29, 2010 by a Female patient taking Augmentin (View Usage) (Dosage: ) . Location: FRANCE , 55 years of age, Patient experienced the following unwanted or unexpected effects: jaundice (What is jaundice?), mixed liver injury.

6570836-X | Abdominal Pain Upper, Diarrhoea, Fatigue, Sensation Of Foreign Body, Urticaria
on Feb 02, 2010 Female patient from UNITED STATES , 61 years of age, weighting 158.0 lb, was diagnosed with sinusitis (What is sinusitis?) and was treated with Augmentin (View Usage). Patient had the following side effects: abdominal pain upper, diarrhoea, fatigue, sensation of foreign body, urticaria. Augmentin dosage: 1 2xday Po.

6566879-2 | Diarrhoea, Hypoglycaemia
on Jan 25, 2010 Female patient from GREECE , 77 years of age, was diagnosed with urinary tract infection (What is urinary tract infection?) and was treated with Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: diarrhoea, hypoglycaemia. Augmentin dosage: . During the same period patient was treated with SOLOSA (View Solosa Review and Solosa Label ).

6554977-9 | Grand Mal Convulsion
Patient was taking Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: grand mal convulsion on Jan 26, 2010 from UNITED STATES Additional patient health information: Male patient , 49 years of age, weighting 135.0 lb, was diagnosed with cellulitis (What is cellulitis?) and. Augmentin dosage: 875-mg Tablets Twice Daily Po. Patient was hospitalized.

6552677-2 | Allergy Test Positive, Anaphylactic Shock
Adverse event was reported on Jan 19, 2010 by a Male patient taking Augmentin (View Usage) (Dosage: ) . Location: FRANCE , 71 years of age, Patient had the following side effects: allergy test positive, anaphylactic shock. Patient was hospitalized.

6550517-9 | Breast Mass, Breast Swelling, Condition Aggravated, Contusion, Discomfort, Dry Skin, Fatigue, Headache, Muscle Atrophy
on Jan 20, 2010 Male patient from UNITED KINGDOM , 63 years of age, was treated with Augmentin (View Usage). After Augmentin was administered, patient had the following side effects: breast mass, breast swelling, condition aggravated, contusion, discomfort, dry skin, fatigue, headache (What is headache?), muscle atrophy. Augmentin dosage: 1g Three Times Per Day. During the same period patient was treated with CHLORHEXIDINE GLUCONATE (View Chlorhexidine Gluconate Review and Chlorhexidine Gluconate Label ), VITAMIN K2 (View Vitamin K2 Review and Vitamin K2 Label ), VITAMINS + MINERALS (View Vitamins + Minerals Review and Vitamins + Minerals Label ).

6547021-0 | Eye Swelling, Hemiparesis, Laryngeal Oedema, Lip Oedema, Respiratory Disorder, Urticaria, Vomiting
on Jan 17, 2010 Female patient from ITALY , 26 years of age, was diagnosed with tonsillitis and was treated with Augmentin (View Usage). Patient experienced the following unwanted or unexpected effects: eye swelling, hemiparesis, laryngeal oedema, lip oedema, respiratory disorder, urticaria, vomiting. Augmentin dosage: 1g Per Day. Patient was hospitalized.

6547015-5 | Clostridial Infection, Diarrhoea
Patient was taking Augmentin (View Usage). Patient had the following side effects: clostridial infection, diarrhoea on Jan 19, 2010 from FRANCE Additional patient health information: Female patient , 90 years of age, was diagnosed with lung infection, productive cough and. Augmentin dosage: . During the same period patient was treated with TIENAM (View Tienam Review and Tienam Label ), TAVANIC (View Tavanic Review and Tavanic Label ), CEFTRIAXONE (View Ceftriaxone Review and Ceftriaxone Label ), TRIATEC (View Triatec Review and Triatec Label ), DIALGIREX (View Dialgirex Review and Dialgirex Label ), LACTULOSE (View Lactulose Review and Lactulose Label ), CARDENSIEL (View Cardensiel Review and Cardensiel Label ), DIFFU K (View Diffu K Review and Diffu K Label ). Patient was hospitalized.