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Amoclav Side Effects

Common Amoclav Side Effects

The most commonly reported Amoclav side effects (click to view or check a box to report):

Gamma-glutamyltransferase Increased (3)
Diarrhoea (3)
Alanine Aminotransferase Increased (2)
Aggression (2)
Amnesia (2)
Aspartate Aminotransferase Increased (2)
Blood Cholesterol Increased (2)
Blood Alkaline Phosphatase Increased (2)
Blood Lactate Dehydrogenase Increased (2)
Areflexia (2)
Cholestasis (2)
Hypokalaemia (2)
Hyperbilirubinaemia (2)
Toxic Epidermal Necrolysis (2)
Hypothyroidism (2)
Jaundice (2)
Stevens-johnson Syndrome (2)
Loss Of Consciousness (2)
Metabolic Acidosis (1)
Muscle Spasms (1)

➢ More



If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

Amoclav Side Effects Reported to FDA

The following Amoclav reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.


The appearance of Amoclav on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.
Blood Creatinine Increased
on Mar 25, 2014 Female from DE , 82 years of age, weighting 152.1 lb, was diagnosed with and was treated with Amoclav. Directly after, patient experienced the unwanted or unexpected Amoclav side effects: blood creatinine increased. Amoclav dosage: N/A.
Associated medications used:
  • Vimpat (Daily Dose: 100 Mg Millgram(s) Every Days)


Hypertension, Muscle Spasms, Influenza Like Illness, Pyrexia, Hyperhidrosis, Lymphadenopathy, Musculoskeletal Pain, Pain In Extremity, Back Pain
Patient was taking Amoclav Plus. Patient felt the following Amoclav side effects: hypertension, muscle spasms, influenza like illness, pyrexia, hyperhidrosis, lymphadenopathy, musculoskeletal pain, pain in extremity, back pain on Nov 05, 2013 from DE Additional patient health information: Female , 74 years of age, weighting 121.3 lb, was diagnosed with and. Amoclav Plus dosage: 500 Mg, Tid.

Metabolic Acidosis, Acute Hepatic Failure
Adverse event was reported on May 29, 2013 by a Male taking Amoclav (Dosage: 2x1 Df With 875 Mg Amoxicillin And 125 Mg Clavulanate/day) was diagnosed with and. Location: DE , 45 years of age, weighting 172.0 lb, After Amoclav was administered, patient encountered several Amoclav side effects: metabolic acidosis, acute hepatic failure.
Multiple concurrent drugs taken:
  • Targin (1 Df, Bid)
  • Viani (2x2)
  • Aclidinium Bromide (2x1)


Stevens-johnson Syndrome, Hypothyroidism, Hypokalaemia
on Oct 10, 2012 Female from DE , 56 years of age, was diagnosed with and was treated with Amoclav 875mg. Directly after, patient experienced the unwanted or unexpected Amoclav side effects: stevens-johnson syndrome, hypothyroidism, hypokalaemia. Amoclav 875mg dosage: N/A.
Associated medications used:
  • Meloxicam



Hypothyroidism, Hypokalaemia, Stevens-johnson Syndrome
on Oct 02, 2012 Female from DE , 56 years of age, was diagnosed with and was treated with Amoclav. Patient felt the following Amoclav side effects: hypothyroidism, hypokalaemia, stevens-johnson syndrome. Amoclav dosage: N/A.
Multiple prescriptions taken:
  • Meloxicam


Crying, Nausea, Lethargy, Nightmare
Patient was taking Amoclav. After Amoclav was administered, patient encountered several Amoclav side effects: crying, nausea, lethargy, nightmare on Nov 02, 2011 from IRELAND Additional patient health information: Male , 24 years of age, weighting 260.1 lb, was diagnosed with and. Amoclav dosage: Daily Dose 1875 Mg.
Multiple concurrent drugs taken:
  • Avelox (Daily Dose 400 Mg)


Abdominal Pain, Blood Pressure Immeasurable, Circulatory Collapse, Dehydration, Diarrhoea, Haematochezia
Adverse event was reported on Jan 25, 2010 by a Female taking Amoclav (Dosage: 1000mg Twice Per Day) was diagnosed with and. Location: GERMANY , 85 years of age, weighting 154.3 lb, Directly after, patient experienced the unwanted or unexpected Amoclav side effects: abdominal pain, blood pressure immeasurable, circulatory collapse, dehydration, diarrhoea, haematochezia.
Associated medications used:
  • Ampicillin And Sulbactam (3g Per Day)
  • Beloc Zok (47.5mg Twice Per Day)
  • Ramipril (2.5mg Per Day)
  • Stangyl (25mg Per Day)
  • Simvastatin (40mg Per Day)
  • Aspirin (100mg Per Day)
Patient was hospitalized.

Toxic Epidermal Necrolysis
on May 29, 2009 Female from GERMANY , 94 years of age, weighting 109.1 lb, was diagnosed with and was treated with Amoclav (amoxicillin, Clavulanate) Film-coated. Patient felt the following Amoclav side effects: toxic epidermal necrolysis. Amoclav (amoxicillin, Clavulanate) Film-coated dosage: 1 Df, Bid, Oral.
Multiple prescriptions taken:
  • Oxazepam
  • Ramipril


Toxic Epidermal Necrolysis
on Jun 02, 2009 Female from GERMANY , 94 years of age, weighting 109.1 lb, was diagnosed with and was treated with Amoclav. After Amoclav was administered, patient encountered several Amoclav side effects: toxic epidermal necrolysis. Amoclav dosage: 1000mg Twice Per Day.
Multiple concurrent drugs taken:
  • Oxazepam
  • Ramipril (10mg Per Day)


Rheumatoid Arthritis
Patient was taking Amoclav. Directly after, patient experienced the unwanted or unexpected Amoclav side effects: rheumatoid arthritis on Jan 31, 2008 from GERMANY Additional patient health information: Female , 67 years of age, was diagnosed with and. Amoclav dosage: N/A.

Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Cholesterol Increased, Diarrhoea, Gamma-glutamyltransferase Increased, Glutamate Dehydrogenase Increased, Hyperbilirubinaemia, Jaundice
Adverse event was reported on Jul 31, 2007 by a Male taking Amoclav (ngx)(amoxicillin, Clavulanate) Film-coated Tablet, 875/125mg (Dosage: 875/125 Mg, Bid, Oral) was diagnosed with and. Location: GERMANY , 55 years of age, weighting 185.2 lb, Patient felt the following Amoclav side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood cholesterol increased, diarrhoea, gamma-glutamyltransferase increased, glutamate dehydrogenase increased, hyperbilirubinaemia, jaundice.

Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Cholesterol Increased, Blood Lactate Dehydrogenase Increased, Diarrhoea, Gamma-glutamyltransferase Increased, Hepatic Enzyme Increased, Hyperbilirubinaemia, Jaundice
on Aug 01, 2007 Male from GERMANY , 55 years of age, was treated with Amoclav. After Amoclav was administered, patient encountered several Amoclav side effects: bilirubin conjugated increased, blood alkaline phosphatase increased, blood cholesterol increased, blood lactate dehydrogenase increased, diarrhoea, gamma-glutamyltransferase increased, hepatic enzyme increased, hyperbilirubinaemia, jaundice. Amoclav dosage: 1000mg Twice Per Day.

Diarrhoea Haemorrhagic
on Jun 04, 2007 Female from GERMANY , 40 years of age, was treated with Amoclav. Directly after, patient experienced the unwanted or unexpected Amoclav side effects: diarrhoea haemorrhagic. Amoclav dosage: N/A.

Amnesia, Areflexia, Loss Of Consciousness
Patient was taking Amoclav (ngx) (amoxicillin, Clavulanate) Film-coated Tablet. Patient felt the following Amoclav side effects: amnesia, areflexia, loss of consciousness on Mar 20, 2007 from GERMANY Additional patient health information: Female , 66 years of age, was diagnosed with and. Amoclav (ngx) (amoxicillin, Clavulanate) Film-coated Tablet dosage: Oral. Patient was hospitalized.

Aggression, Restlessness
Adverse event was reported on Mar 27, 2007 by a Female taking Amoclav (Dosage: 625mg Three Times Per Day) . Location: GERMANY , 51 years of age, After Amoclav was administered, patient encountered several Amoclav side effects: aggression, restlessness.
Multiple concurrent drugs taken:
  • Levothyroxine Sodium


Amnesia, Areflexia, Loss Of Consciousness
on Mar 22, 2007 Female from GERMANY , 66 years of age, was treated with Amoclav. Directly after, patient experienced the unwanted or unexpected Amoclav side effects: amnesia, areflexia, loss of consciousness. Amoclav dosage: N/A. Patient was hospitalized.

Cholestasis
on Mar 17, 2006 Female from GERMANY , 36 years of age, was diagnosed with and was treated with Amoclav. Patient felt the following Amoclav side effects: cholestasis. Amoclav dosage: 625mg Per Day. Patient was hospitalized.

Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Cholestasis, Gamma-glutamyltransferase Increased
Patient was taking Amoclav. After Amoclav was administered, patient encountered several Amoclav side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood lactate dehydrogenase increased, cholestasis, gamma-glutamyltransferase increased on Mar 07, 2006 from GERMANY Additional patient health information: Female , 36 years of age, was diagnosed with and. Amoclav dosage: 625mg Per Day. Patient was hospitalized.

Cholelithiasis
Adverse event was reported on Mar 17, 2006 by a Female taking Amoclav (Dosage: 625mg Per Day) was diagnosed with and. Location: GERMANY , 36 years of age, Directly after, patient experienced the unwanted or unexpected Amoclav side effects: cholelithiasis. Patient was hospitalized.

Dermatitis Bullous, Dysphagia, Dyspnoea, Oral Mucosal Blistering
on Mar 17, 2006 Male from GERMANY , 20 years of age, weighting 180.8 lb, was diagnosed with and was treated with Amoclav. Patient felt the following Amoclav side effects: dermatitis bullous, dysphagia, dyspnoea, oral mucosal blistering. Amoclav dosage: 1000mg Twice Per Day.

Aggression, Insomnia, Psychomotor Hyperactivity
on Jan 16, 2006 Male from GERMANY , child 5 years of age, was diagnosed with and was treated with Amoclav. After Amoclav was administered, patient encountered several Amoclav side effects: aggression, insomnia, psychomotor hyperactivity. Amoclav dosage: N/A.

Keep Track of Side Effects

Note Your Observations

It is really important to keep of your symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:

     

    Side Effects

    Scale

    Date & Time

    Other Medicine(s) or Treatment(s)

     

     

     

     

    Scale: 1 = very mild to 10 = very bad


    Track Online

  • User Sign In
  • Register to track your side effects

  • You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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    Safety Alerts, Active Ingredients, Usage Information

    More About Amoclav

    Side Effects reported to FDA: 21

    Amoclav safety alerts: No

    Reported deaths: 2

    Reported hospitalizations: 5

    Latest Amoclav clinical trials