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Augmentin International Normalised Ratio Increased Side Effects

Augmentin International Normalised Ratio Increased Side Effect Reports


The following Augmentin International Normalised Ratio Increased side effect reports were submitted by healthcare professionals and consumers.

This information will help you understand how side effects, such as International Normalised Ratio Increased, can occur, and what you can do about them.

A side effect could appear soon after you start Augmentin or it might take time to develop.



Bronchitis, Malaise, International Normalised Ratio Increased, Loss Of Consciousness

This International Normalised Ratio Increased side effect was reported by a physician from FRANCE. A 86-year-old female patient (weight:NA) experienced the following symptoms/conditions: bronchitis. The patient was prescribed Augmentin (dosage: NA), which was started on Apr 24, 2012. Concurrently used drugs:
  • Aricept
  • Coumadin
  • Citalopram
  • Memantine Hydrochloride
  • Moxifloxacin Hcl
  • Furosemide
  • Lisinopril
When starting to take Augmentin the consumer reported the following symptoms:
  • Bronchitis
  • Malaise
  • International Normalised Ratio Increased
  • Loss Of Consciousness
The patient was hospitalized. These side effects may potentially be related to Augmentin.
Muscle Haemorrhage, Anaemia, International Normalised Ratio Increased

This International Normalised Ratio Increased Augmentin '125' side effect was reported by a health professional from FRANCE on Apr 02, 2012. A male , 83 years of age, was diagnosed with and was treated with Augmentin '125'. The patient presented the following health conditions:
  • Muscle Haemorrhage
  • Anaemia
  • International Normalised Ratio Increased
. Augmentin '125' dosage: 1 G, Tid. Additional drugs used at the same time:
  • Previscan (Unk)
  • Ciprofloxacin Hydrochloride (400 Mg, Bid)
The patient was hospitalized.
International Normalised Ratio Increased

This is a Augmentin '125' side effect report of a 84-year-old female patient (weight:NA) from SWITZERLAND, suffering from the following symptoms/conditions: NA, who was treated with Augmentin '125' (dosage:NA, start time: Jan 01, 2012), combined with:
  • Esidrix
  • Cordarone
  • Nexium
  • Irbesartan
  • Sintrom (As Necessary)
  • Clarithromycin
  • Imipenem And Cilastatin Sodium
  • Metoprolol Tartrate And Hydrochlorothiazide
, and developed a serious reaction and a International Normalised Ratio Increased side effect. The patient presented with:
  • International Normalised Ratio Increased
which developed after the beginning of treatment. The patient was hospitalized. This side effect report can indicate a possible existence of increased vulnerability to Augmentin '125' treatment in female patients suffering from NA, resulting in International Normalised Ratio Increased.

Alanine Aminotransferase Increased, Gamma-glutamyltransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, International Normalised Ratio Increased, Aspartate Aminotransferase Increased

A 74-year-old patient (weight: NA) from SWITZERLAND with the following symptoms: NA started Augmentin '125' treatment (dosage: 2.2 G, 3x/day) on Jul 26, 2011. Soon after starting Augmentin '125' treatment, the consumer experienced several side effects, including:
  • Alanine Aminotransferase Increased
  • Gamma-glutamyltransferase Increased
  • Blood Alkaline Phosphatase Increased
  • Blood Bilirubin Increased
  • International Normalised Ratio Increased
  • Aspartate Aminotransferase Increased
. Concurrently used drugs:
  • Atorvastatin Calcium (20 Mg, 1x/day)
  • Aspirin (100 Mg, 1x/day)
  • Nexium (20 Mg, 1x/day)
  • Amoxicillin (750 Mg, 3x/day)
  • Marcumar (Unk)
  • Norvasc (5 Mg, 1x/day)
  • Clindamycin Hcl (600 Mg, 3x/day)
  • Ramipril (10 Mg, 1x/day)
The patient was hospitalized. This finding indicates that some patients can be more vulnerable to developing Augmentin '125' side effects, such as International Normalised Ratio Increased.
International Normalised Ratio Increased, Subdural Haematoma

A female patient from NETHERLANDS was prescribed and started Augmentin '125' on May 07, 2009. Patient felt the following Augmentin side effects: international normalised ratio increased, subdural haematoma Additional patient health information: Female , weighting 163.1 lb, The consumer reported the following symptoms: . Augmentin '125' dosage: 825mg Three Times Per Day. Concurrently used drugs:
  • Acenocoumarol
  • Omeprazole (20mg Per Day)
  • Paracetamol (1000mg Four Times Per Day)
  • Diclofenac (50mg Per Day)
  • Triamterene And Hydrochlorothiazide
  • Selokeen (50mg Twice Per Day)
  • Novomix (100iu Twice Per Day)
The patient was hospitalized.
Deep Vein Thrombosis, International Normalised Ratio Increased, Oedema Peripheral, Pain, Prothrombin Time Prolonged

This report suggests a potential Augmentin '125' International Normalised Ratio Increased side effect(s) that can have serious consequences. A 25-year-old female patient from FRANCE (weight:NA) was diagnosed with the following health condition(s): NA and used Augmentin '125' (dosage: 1g Three Times Per Day) starting Mar 15, 2009. Soon after starting Augmentin '125' the patient began experiencing various side effects, including:
  • Deep Vein Thrombosis
  • International Normalised Ratio Increased
  • Oedema Peripheral
  • Pain
  • Prothrombin Time Prolonged
Drugs used concurrently:
  • Tavanic (500mg Per Day)
  • Innohep
The patient was hospitalized. Although Augmentin '125' demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as International Normalised Ratio Increased, may still occur.
Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Cholestasis, Gamma-glutamyltransferase Increased, Haematoma, International Normalised Ratio Increased

An adverse event was reported by a consumer or non-health professional on Mar 20, 2009 by a Female taking Augmentin '125' (dosage: 1g Three Times Per Day) was diagnosed with and. Location: FRANCE , 81 years of age, patient began experiencing various side effects, including: Directly after treatment started, patient experienced the unwanted or unexpected Augmentin side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, cholestasis, gamma-glutamyltransferase increased, haematoma, international normalised ratio increased. Additional medications/treatments:
Associated medications used:
  • Coumadin
  • Neurontin (800mg Three Times Per Day)
  • Depakene (500mg See Dosage Text)
  • Diffu K
  • Seresta (5mg Per Day)
  • Oramorph Sr
  • Duragesic-100
  • Dafalgan
International Normalised Ratio Increased, Overdose

This International Normalised Ratio Increased problem was reported by a consumer or non-health professional from FRANCE. A 81-year-old patient (weight: NA) was diagnosed with the following medical condition(s): bronchitis.On Jan 01, 2009 a consumer started treatment with Augmentin '125' (dosage: NA). The following drugs/medications were being taken at the same time:
  • Previscan (20mg Per Day)
  • Cordarone
  • Pravastatin
  • Tamsulosine
When commencing Augmentin '125', the patient experienced the following unwanted symptoms /side effects:
  • International Normalised Ratio Increased
  • Overdose
The patient was hospitalized. Although all drugs are carefully tested before they are licensed for use, they carry potential side effect risks. Some side effects, such as International Normalised Ratio Increased, may become evident only after a product is in use by the general population.
Hypoprothrombinaemia, International Normalised Ratio Increased

This is a Augmentin '125' side effect report of a 90-year-old female patient (weight: NA) from FRANCE. The patient developed the following symptoms/conditions: NA and was treated with Augmentin '125' (dosage: 2unit Twice Per Day) starting Dec 16, 2008. Concurrently used drugs:
  • Previscan (20mg Per Day)
  • Doliprane (500mg As Required)
  • Plavix
  • Kenzen
  • Furosemide
  • Ramipril
  • Effexor
  • Sulpiride
Soon after that, the consumer experienced the following of symptoms:
  • Hypoprothrombinaemia
  • International Normalised Ratio Increased
The patient was hospitalized. This opens a possibility that Augmentin '125' could cause International Normalised Ratio Increased and that some female patients may be more susceptible.
International Normalised Ratio Increased

This International Normalised Ratio Increased side effect was reported by a consumer or non-health professional from FRANCE on Jan 21, 2009. A patient from FRANCE , 81 years of age, was diagnosed with and was treated with Augmentin '125'. Directly after treatment started, patient experienced the unwanted or unexpected Augmentin side effects: international normalised ratio increased. Augmentin '125' dosage: 1g Three Times Per Day.
Associated medications used:
  • Previscan
  • Crestor (5mg Per Day)
  • Di Antalvic
  • Doliprane (500mg Twice Per Day)
  • Triatec
  • Amlod
  • Insulatard (16iu Twice Per Day)
  • Leuprolide Acetate
The patient was hospitalized. These side effects may potentially be related to Augmentin '125'.
Clostridium Difficile Colitis, Diarrhoea, Hyponatraemia, International Normalised Ratio Increased, Leukocytosis, Mucous Stools, Pseudomembranous Colitis, Rectal Haemorrhage

This International Normalised Ratio Increased side effect was reported by a consumer or non-health professional from FRANCE. A 95-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA. The patient was prescribed Augmentin '125' (dosage: 1g Twice Per Day), which was started on Jul 10, 2008. Concurrently used drugs:
  • Flagyl (250mg Four Times Per Day)
  • Previscan (.25unit Per Day)
  • Hemigoxine
  • Levothyrox (100mcg Per Day)
  • Atarax (12.5mg Per Day)
  • Lasilix (40mg Per Day)
  • Duspatalin
  • Athymil (10mg Twice Per Day)
When starting to take Augmentin '125' the consumer reported the following symptoms:
  • Clostridium Difficile Colitis
  • Diarrhoea
  • Hyponatraemia
  • International Normalised Ratio Increased
  • Leukocytosis
  • Mucous Stools
  • Pseudomembranous Colitis
  • Rectal Haemorrhage
The patient was hospitalized. These side effects may potentially be related to Augmentin '125'.
Haematuria, International Normalised Ratio Increased, Prothrombin Time Ratio Decreased

This International Normalised Ratio Increased Augmentin '125' side effect was reported by a consumer or non-health professional from FRANCE on Jan 19, 2009. A Female , 69 years of age, was treated with Augmentin '125'. The patient presented the following health conditions:
  • Haematuria
  • International Normalised Ratio Increased
  • Prothrombin Time Ratio Decreased
. Augmentin '125' dosage: 1g Three Times Per Day. Additional drugs used at the same time:
  • Coumadin (2.5mg Per Day)
  • Zeclar (500mg Twice Per Day)
The patient was hospitalized.
International Normalised Ratio Increased, Prothrombin Time Ratio Decreased

This is a Augmentin '125' side effect report of a 78-year-old patient (weight:NA) from FRANCE, suffering from the following symptoms/conditions: NA, who was treated with Augmentin '125' (dosage:NA, start time: Sep 11, 2008), combined with:
  • Previscan
  • Solu-medrol
  • Loxen
  • Cordarone
  • Lasix
  • Topalgic ( France )
  • Myolastan
  • Micardis
, and developed a serious reaction and a International Normalised Ratio Increased side effect. The patient presented with:
  • International Normalised Ratio Increased
  • Prothrombin Time Ratio Decreased
which developed after the beginning of treatment. The patient was hospitalized. This side effect report can indicate a possible existence of increased vulnerability to Augmentin '125' treatment in patients suffering from NA, resulting in International Normalised Ratio Increased.
International Normalised Ratio Increased, Prothrombin Time Ratio Decreased

A 78-year-old patient (weight: NA) from FRANCE with the following symptoms: NA started Augmentin '125' treatment (dosage: NA) on Sep 11, 2008. Soon after starting Augmentin '125' treatment, the consumer experienced several side effects, including:
  • International Normalised Ratio Increased
  • Prothrombin Time Ratio Decreased
. Concurrently used drugs:
  • Previscan
  • Solu-medrol
  • Loxen
  • Cordarone
  • Lasix
  • Topalgic ( France )
  • Myolastan
  • Micardis
The patient was hospitalized. This finding indicates that some patients can be more vulnerable to developing Augmentin '125' side effects, such as International Normalised Ratio Increased.
Dyspnoea, International Normalised Ratio Increased, Overdose, Pleural Effusion

A female patient from FRANCE was prescribed and started Augmentin '125' on Jul 04, 2008. After Augmentin was administered, patient encountered several Augmentin side effects: dyspnoea, international normalised ratio increased, overdose, pleural effusion Additional patient health information: Female , 81 years of age, The consumer reported the following symptoms: . Augmentin '125' dosage: NA. Concurrently used drugs:
  • Previscan
  • Calciparine (.6ml Twice Per Day)
  • Cordarone (1tab Per Day)
  • Tahor (1tab Per Day)
  • Praxilene 200
  • Acetaminophen
  • Lorazepam
The patient was hospitalized.
Anaemia, Conjunctival Discolouration, Epistaxis, Heart Sounds Abnormal, International Normalised Ratio Increased, Pallor, Rales

This report suggests a potential Augmentin '125' International Normalised Ratio Increased side effect(s) that can have serious consequences. A 67-year-old female patient from FRANCE (weight:NA) was diagnosed with the following health condition(s): NA and used Augmentin '125' (dosage: 3g Per Day) starting Apr 24, 2008. Soon after starting Augmentin '125' the patient began experiencing various side effects, including:
  • Anaemia
  • Conjunctival Discolouration
  • Epistaxis
  • Heart Sounds Abnormal
  • International Normalised Ratio Increased
  • Pallor
  • Rales
Drugs used concurrently:
  • Previscan (30mg Per Day)
  • Cordarone
  • Perindopril Erbumine (1tab Per Day)
  • Vitamine B12 (3mg Weekly)
  • Lasix (.5tab Per Day)
  • Bisoprolol Fumarate (1tab Alternate Days)
The patient was hospitalized. Although Augmentin '125' demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as International Normalised Ratio Increased, may still occur.
International Normalised Ratio Increased

An adverse event was reported by a consumer or non-health professional on Jun 16, 2008 by a Female taking Augmentin '125' (dosage: 2g Per Day) . Location: FRANCE , 94 years of age, patient began experiencing various side effects, including: Patient felt the following Augmentin side effects: international normalised ratio increased. Additional medications/treatments:
Multiple prescriptions taken:
  • Previscan (5mg Per Day)
  • Morphine
  • Forlax
  • Renitec
  • Paroxetine Hcl
  • Cordarone
  • Amlor
  • Lasix
The patient was hospitalized.
International Normalised Ratio Increased, Purpura

This International Normalised Ratio Increased problem was reported by a consumer or non-health professional from FRANCE. A 87-year-old female patient (weight: NA) was diagnosed with the following medical condition(s): pyelonephritis acute,atrial fibrillation.On Apr 06, 2008 a consumer started treatment with Augmentin '125' (dosage: NA). The following drugs/medications were being taken at the same time:
  • Previscan
  • Tavanic
  • Digoxin
  • Cardensiel (5mg Per Day)
  • Tardyferon
When commencing Augmentin '125', the patient experienced the following unwanted symptoms /side effects:
  • International Normalised Ratio Increased
  • Purpura
Although all drugs are carefully tested before they are licensed for use, they carry potential side effect risks. Some side effects, such as International Normalised Ratio Increased, may become evident only after a product is in use by the general population.
Haematochezia, Haematuria, International Normalised Ratio Increased, Prothrombin Time Ratio Decreased

This is a Augmentin '125' side effect report of a 69-year-old female patient (weight: NA) from FRANCE. The patient developed the following symptoms/conditions: bronchopneumopathy and was treated with Augmentin '125' (dosage: 1g Three Times Per Day) starting Mar 07, 2008. Concurrently used drugs:
  • Coumadin (7mg Per Day)
  • Zeclar (500mg Twice Per Day)
  • Verapamil
Soon after that, the consumer experienced the following of symptoms:
  • Haematochezia
  • Haematuria
  • International Normalised Ratio Increased
  • Prothrombin Time Ratio Decreased
The patient was hospitalized. This opens a possibility that Augmentin '125' could cause International Normalised Ratio Increased and that some female patients may be more susceptible.
International Normalised Ratio Increased

This International Normalised Ratio Increased side effect was reported by a consumer or non-health professional from FRANCE on Apr 22, 2008. A patient from FRANCE , 81 years of age, was diagnosed with and was treated with Augmentin '125'. Patient felt the following Augmentin side effects: international normalised ratio increased. Augmentin '125' dosage: 1g Three Times Per Day.
Multiple prescriptions taken:
  • Doliprane (500mg Twice Per Day)
  • Previscan
  • Crestor (5mg Per Day)
  • Diantalvic
  • Triatec (5mg Per Day)
  • Amlor (10mg Per Day)
  • Insulatard (16iu Twice Per Day)
  • Leuprolide Acetate (1inj Every 3 Months)
The patient was hospitalized. These side effects may potentially be related to Augmentin '125'.
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DISCLAIMER: ALL DATA PROVIDED AS-IS, refer to terms of use for additional information.

Augmentin International Normalised Ratio Increased Causes and Reviews


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Augmentin International Normalised Ratio Increased Reviews

Sat, 13 Aug 2011

ive been taken for 3 days and now i experience sore throat,,tired and some rashes to my private part,,,that sucks

Mon, 11 Apr 2011

I had a throat and gun infection at the same time. My doc gave me augmenten for remedy.My last dose was more than 5 days back but still i am suffering from its side affects and feeling diziness confusion. augmented screwed me big time as i am not able to concentrate on almost anything :-( however, during my dosage period i observed frequent rashes appearing on the ears, face and on some areas of the arms. the rashes were punctual as they hit me daily for 3 to 4 days at the same time period. I tool 635 Mg 12 tablests in total for 4 days = 3 tabs daily....anyone knows how much more these deadly side affects will last? or what to do for eliminating attaks on nervous system?

Mon, 25 Apr 2011

I have been constipated, is that a symptom????

Sat, 26 Mar 2011

My five year old has had vasculitis for two weeks which his doctors have attributed to a single dose of Augmentin. They are testing him like crazy for serious problems and monitoring his kidney function closely, meanwhile he has a horrible rash that just seems to get worse as time goes by. I have no idea what else I can do to help my baby - I am terrified for him.

Wed, 17 Nov 2010

Augmentin 625: 2x a day
I've been on it for 2 days. Experienced unexplained joint pains and swelling of my hands, feet face. Can see flashes on my left eye on the 2nd day. Have also noticed that I always want to eat.

Sat, 08 Aug 2009
Due to elevated liver enzyme levels and an elevated ANA, my previous doctor gave me a diagnosis of autoimmune hepatitis. After reviewing my charts, my current doctor believes that it was an autoimmune response to 3 back-to-back courses of amoxicillin then a course of Augmentin to treat a sinus infection. I read somewhere that Augmentin has been shown to cause or has been linked to autoimmune responses. Am I correct? My current doctor is trying to get the autoimmune hepatitis diagnosis removed from my records but I'm having trouble convincing the insurance companies that it was an improper diagnosis. Is there evidence I can give them to support my and my doc's possition.
Fri, 30 Apr 2010
can Augmentine 625 mg twice daily for five days cause as a side effect Hyperthermia
DISCLAIMER: ALL DATA PROVIDED AS-IS, refer to terms of use for additional information.

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Top Augmentin Side Effects

Diarrhoea (341)
Pruritus (324)
Rash (236)
Pyrexia (227)
Jaundice (205)
Erythema (198)
Alanine Aminotransferase Increased (194)
Dyspnoea (186)
Urticaria (180)
Anaphylactic Shock (179)
Vomiting (173)
Aspartate Aminotransferase Increased (168)
Blood Alkaline Phosphatase Increased (164)
Nausea (152)
Abdominal Pain (145)
Hypotension (136)
Cholestasis (136)
Hepatitis Cholestatic (134)
Gamma-glutamyltransferase Increased (130)
Malaise (119)
Hypersensitivity (113)
Blood Bilirubin Increased (108)
Rash Maculo-papular (104)
Face Oedema (103)
Asthenia (98)
Hepatitis (96)
Toxic Skin Eruption (92)
Abdominal Pain Upper (89)
Anaphylactic Reaction (86)
Renal Failure Acute (79)
Chromaturia (78)
Oedema Peripheral (74)
Eosinophilia (74)
Purpura (73)
Angioedema (73)
Dizziness (71)
Anaemia (69)
Bronchospasm (69)
International Normalised Ratio Increased (69)
Thrombocytopenia (67)
Tachycardia (66)
Rash Erythematous (65)
Inflammation (63)
Oedema (63)
Fatigue (61)
Pain (54)
Dehydration (54)
Anorexia (53)
Death (53)
Blood Pressure Decreased (53)

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