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Amoclav Side Effects

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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.

Amoclav Side Effects Reported to FDA



Amoclav Side Effect Report#9879338
Blood Creatinine Increased
This is a report of a 82-year-old female patient (weight: NA) from DE, suffering from the following health symptoms/conditions: pneumonia,epilepsy, who was treated with Amoclav (dosage: NA, start time:
Jan 23, 2014), combined with:
  • Vimpat (Daily Dose: 100 Mg Millgram(s) Every Days)
and developed a serious reaction and side effect(s): Blood Creatinine Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Amoclav treatment in female patients, resulting in Blood Creatinine Increased side effect.
Amoclav Side Effect Report#9606020
Hypertension, Muscle Spasms, Influenza Like Illness, Pyrexia, Hyperhidrosis, Lymphadenopathy, Musculoskeletal Pain, Pain In Extremity, Back Pain
This report suggests a potential Amoclav Plus Hypertension side effect(s) that can have serious consequences. A 74-year-old female patient (weight: NA) from DE was diagnosed with the following symptoms/conditions: dental disorder prophylaxis and used Amoclav Plus (dosage: 500 Mg, Tid) starting
Sep 28, 2013. After starting Amoclav Plus the patient began experiencing various side effects, including: Hypertension, Muscle Spasms, Influenza Like Illness, Pyrexia, Hyperhidrosis, Lymphadenopathy, Musculoskeletal Pain, Pain In Extremity, Back PainAdditional drugs used concurrently: NA. Although Amoclav Plus demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hypertension, may still occur.
Amoclav Side Effect Report#9314874
Metabolic Acidosis, Acute Hepatic Failure
This Metabolic Acidosis problem was reported by a health professional from DE. A 45-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: chronic obstructive pulmonary disease,dyspnoea. On
Apr 11, 2013 this consumer started treatment with Amoclav (dosage: 2x1 Df With 875 Mg Amoxicillin And 125 Mg Clavulanate/day). The following drugs were being taken at the same time:
  • Targin (1 Df, Bid)
  • Viani (2x2)
  • Aclidinium Bromide (2x1)
When using Amoclav, the patient experienced the following unwanted symptoms/side effects: Metabolic Acidosis, Acute Hepatic FailureAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Metabolic Acidosis, may become evident only after a product is in use by the general population.
Amoclav Side Effect Report#8833400
Stevens-johnson Syndrome, Hypothyroidism, Hypokalaemia
This Stevens-johnson Syndrome side effect was reported by a physician from DE. A 56-year-old female patient (weight:NA) experienced the following symptoms/conditions: tooth disorder,pain.The patient was prescribed Amoclav 875mg (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Meloxicam
.After starting to take Amoclav 875mg the consumer reported adverse symptoms, such as: Stevens-johnson Syndrome, Hypothyroidism, HypokalaemiaThese side effects may potentially be related to Amoclav 875mg.
Amoclav Side Effect Report#8821472
Hypothyroidism, Hypokalaemia, Stevens-johnson Syndrome
This is a report of a 56-year-old female patient (weight: NA) from DE, suffering from the following health symptoms/conditions: tooth disorder,pain, who was treated with Amoclav (dosage: NA, start time: NS), combined with:
  • Meloxicam
and developed a serious reaction and side effect(s): Hypothyroidism, Hypokalaemia, Stevens-johnson Syndrome after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Amoclav treatment in female patients, resulting in Hypothyroidism side effect.
Amoclav Side Effect Report#7905186-X
Crying, Nausea, Lethargy, Nightmare
This report suggests a potential Amoclav Crying side effect(s) that can have serious consequences. A 24-year-old male patient (weight: NA) from Ireland was diagnosed with the following symptoms/conditions: infected dermal cyst,respiratory tract infection and used Amoclav (dosage: Daily Dose 1875 Mg) starting
Oct 19, 2011. After starting Amoclav the patient began experiencing various side effects, including: Crying, Nausea, Lethargy, NightmareAdditional drugs used concurrently:
  • Avelox (Daily Dose 400 Mg)
Although Amoclav demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Crying, may still occur.
Amoclav Side Effect Report#6556449-4
Abdominal Pain, Blood Pressure Immeasurable, Circulatory Collapse, Dehydration, Diarrhoea, Haematochezia
This Abdominal Pain problem was reported by a consumer or non-health professional from Germany. A 85-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: erysipelas. On
Jan 01, 2006 this consumer started treatment with Amoclav (dosage: 1000mg Twice Per Day). The following drugs were being taken at the same time:
  • 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)
When using Amoclav, the patient experienced the following unwanted symptoms/side effects: Abdominal Pain, Blood Pressure Immeasurable, Circulatory Collapse, Dehydration, Diarrhoea, HaematocheziaThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Abdominal Pain, may become evident only after a product is in use by the general population.
Amoclav Side Effect Report#6216991-2
Toxic Epidermal Necrolysis
This Toxic Epidermal Necrolysis side effect was reported by a physician from Germany. A 94-year-old female patient (weight:NA) experienced the following symptoms/conditions: skin lesion.The patient was prescribed Amoclav (amoxicillin, Clavulanate) Film-coated (drug dosage: 1 Df, Bid, Oral), which was initiated on NS. Concurrently used drugs:
  • Oxazepam
  • Ramipril
.After starting to take Amoclav (amoxicillin, Clavulanate) Film-coated the consumer reported adverse symptoms, such as: Toxic Epidermal NecrolysisThese side effects may potentially be related to Amoclav (amoxicillin, Clavulanate) Film-coated.
Amoclav Side Effect Report#6214811-3
Toxic Epidermal Necrolysis
This is a report of a 94-year-old female patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: skin lesion,sleep disorder, who was treated with Amoclav (dosage: 1000mg Twice Per Day, start time:
Mar 01, 2009), combined with:
  • Oxazepam
  • Ramipril (10mg Per Day)
and developed a serious reaction and side effect(s): Toxic Epidermal Necrolysis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Amoclav treatment in female patients, resulting in Toxic Epidermal Necrolysis side effect.
Amoclav Side Effect Report#5612635-9
Rheumatoid Arthritis
This report suggests a potential Amoclav Rheumatoid Arthritis side effect(s) that can have serious consequences. A 67-year-old female patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: pneumonia and used Amoclav (dosage: NA) starting NS. After starting Amoclav the patient began experiencing various side effects, including: Rheumatoid ArthritisAdditional drugs used concurrently: NA. Although Amoclav demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Rheumatoid Arthritis, may still occur.
Amoclav Side Effect Report#5409314-X
Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Cholesterol Increased, Diarrhoea, Gamma-glutamyltransferase Increased, Glutamate Dehydrogenase Increased, Hyperbilirubinaemia, Jaundice
This Alanine Aminotransferase Increased problem was reported by a physician from Germany. A 55-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: bronchitis. On
Mar 31, 2007 this consumer started treatment with Amoclav (ngx)(amoxicillin, Clavulanate) Film-coated Tablet, 875/125mg (dosage: 875/125 Mg, Bid, Oral). The following drugs were being taken at the same time: NA. When using Amoclav (ngx)(amoxicillin, Clavulanate) Film-coated Tablet, 875/125mg, the patient experienced the following unwanted symptoms/side effects: Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Cholesterol Increased, Diarrhoea, Gamma-glutamyltransferase Increased, Glutamate Dehydrogenase Increased, Hyperbilirubinaemia, JaundiceAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Alanine Aminotransferase Increased, may become evident only after a product is in use by the general population.
Amoclav Side Effect Report#5406076-7
Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Cholesterol Increased, Blood Lactate Dehydrogenase Increased, Diarrhoea, Gamma-glutamyltransferase Increased, Hepatic Enzyme Increased, Hyperbilirubinaemia, Jaundice
This Bilirubin Conjugated Increased side effect was reported by a physician from Germany. A 55-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Amoclav (drug dosage: 1000mg Twice Per Day), which was initiated on
Mar 31, 2007. Concurrently used drugs: NA..After starting to take Amoclav the consumer reported adverse symptoms, such as: Bilirubin Conjugated Increased, Blood Alkaline Phosphatase Increased, Blood Cholesterol Increased, Blood Lactate Dehydrogenase Increased, Diarrhoea, Gamma-glutamyltransferase Increased, Hepatic Enzyme Increased, Hyperbilirubinaemia, JaundiceThese side effects may potentially be related to Amoclav.
Amoclav Side Effect Report#5355633-5
Diarrhoea Haemorrhagic
This is a report of a 40-year-old female patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: NA, who was treated with Amoclav (dosage: NA, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Diarrhoea Haemorrhagic after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Amoclav treatment in female patients, resulting in Diarrhoea Haemorrhagic side effect.
Amoclav Side Effect Report#5284427-4
Amnesia, Areflexia, Loss Of Consciousness
This report suggests a potential Amoclav (ngx) (amoxicillin, Clavulanate) Film-coated Tablet Amnesia side effect(s) that can have serious consequences. A 66-year-old female patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: osteitis and used Amoclav (ngx) (amoxicillin, Clavulanate) Film-coated Tablet (dosage: Oral) starting NS. After starting Amoclav (ngx) (amoxicillin, Clavulanate) Film-coated Tablet the patient began experiencing various side effects, including: Amnesia, Areflexia, Loss Of ConsciousnessAdditional drugs used concurrently: NA.The patient was hospitalized. Although Amoclav (ngx) (amoxicillin, Clavulanate) Film-coated Tablet demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Amnesia, may still occur.
Amoclav Side Effect Report#5281784-X
Aggression, Restlessness
This Aggression problem was reported by a health professional from Germany. A 51-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Amoclav (dosage: 625mg Three Times Per Day). The following drugs were being taken at the same time:
  • Levothyroxine Sodium
When using Amoclav, the patient experienced the following unwanted symptoms/side effects: Aggression, RestlessnessAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Aggression, may become evident only after a product is in use by the general population.
Amoclav Side Effect Report#5277288-0
Amnesia, Areflexia, Loss Of Consciousness
This Amnesia side effect was reported by a pharmacist from Germany. A 66-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Amoclav (drug dosage: NA), which was initiated on NS. Concurrently used drugs: NA..After starting to take Amoclav the consumer reported adverse symptoms, such as: Amnesia, Areflexia, Loss Of ConsciousnessThese side effects may potentially be related to Amoclav. The patient was hospitalized.
Amoclav Side Effect Report#5086597-X
Cholestasis
This is a report of a 36-year-old female patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: bronchopneumonia, who was treated with Amoclav (dosage: 625mg Per Day, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Cholestasis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Amoclav treatment in female patients, resulting in Cholestasis side effect. The patient was hospitalized.
Amoclav Side Effect Report#5086596-8
Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Cholestasis, Gamma-glutamyltransferase Increased
This report suggests a potential Amoclav Alanine Aminotransferase Increased side effect(s) that can have serious consequences. A 36-year-old female patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: bronchopneumonia and used Amoclav (dosage: 625mg Per Day) starting NS. After starting Amoclav the patient began experiencing various side effects, including: Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Cholestasis, Gamma-glutamyltransferase IncreasedAdditional drugs used concurrently: NA.The patient was hospitalized. Although Amoclav demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Alanine Aminotransferase Increased, may still occur.
Amoclav Side Effect Report#4951758-4
Cholelithiasis
This Cholelithiasis problem was reported by a physician from Germany. A 36-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: bronchopneumonia. On NS this consumer started treatment with Amoclav (dosage: 625mg Per Day). The following drugs were being taken at the same time: NA. When using Amoclav, the patient experienced the following unwanted symptoms/side effects: CholelithiasisThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Cholelithiasis, may become evident only after a product is in use by the general population.
Amoclav Side Effect Report#4947817-2
Dermatitis Bullous, Dysphagia, Dyspnoea, Oral Mucosal Blistering
This Dermatitis Bullous side effect was reported by a pharmacist from Germany. A 20-year-old male patient (weight:NA) experienced the following symptoms/conditions: tonsillitis.The patient was prescribed Amoclav (drug dosage: 1000mg Twice Per Day), which was initiated on
Feb 01, 2006. Concurrently used drugs: NA..After starting to take Amoclav the consumer reported adverse symptoms, such as: Dermatitis Bullous, Dysphagia, Dyspnoea, Oral Mucosal BlisteringThese side effects may potentially be related to Amoclav.
Amoclav Side Effect Report#4893741-3
Aggression, Insomnia, Psychomotor Hyperactivity
This is a report of a 5-year-old male patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: sinusitis, who was treated with Amoclav (dosage: NA, start time:
Dec 01, 2005), combined with: NA. and developed a serious reaction and side effect(s): Aggression, Insomnia, Psychomotor Hyperactivity after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Amoclav treatment in male patients, resulting in Aggression side effect.



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.

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Track Your Side Effects

Note Your Observations

It is really important to keep track of your health 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

    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.

    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.

    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.

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    Amoclav 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

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