Bioclavid Side Effects

Common Bioclavid Side Effects

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

Alanine Aminotransferase Increased (2)
Pain (2)
Malaise (2)
Headache (2)
Jaundice (2)
Hepatic Enzyme Increased (1)
Spleen Disorder (1)
Haemoglobin Decreased (1)
Aphthous Stomatitis (1)
Rash (1)
Abdominal Pain (1)
Dysphagia (1)
Lip Swelling (1)
Hepatitis (1)
Hepatotoxicity (1)
Hepatic Pain (1)
Hepatic Necrosis (1)
Neck Pain (1)
Liver Disorder (1)
Pyrexia (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.

Bioclavid Side Effects Reported to FDA

The following Bioclavid 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 Bioclavid 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.
Hepatitis, Liver Disorder, Pyrexia, Malaise, Confusional State
This is a report of a 86-year-old male patient (weight: NA) from DK, suffering from the following symptoms/conditions: pneumonia, who was treated with Bioclavid (dosage: NA, start time: Nov 01, 2012), combined with: NA. and developed a serious reaction and side effect(s). The consumer presented with:
  • Hepatitis
  • Liver Disorder
  • Pyrexia
  • Malaise
  • Confusional State
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Bioclavid treatment in male patients, resulting in death side effect. The patient was hospitalized.

Neck Pain, Diplegia, Convulsion, Rash
This report suggests a potential Bioclavid Neck Pain, Diplegia, Convulsion, Rash side effect(s) that can have serious consequences. A 7-year-old male patient (weight: NA) from BE was diagnosed with the following symptoms/conditions: infection prophylaxis and used Bioclavid (dosage: Unk Ukn, Unk) starting NS. Soon after starting Bioclavid the patient began experiencing various side effects, including:
  • Neck Pain
  • Diplegia
  • Convulsion
  • Rash
Drugs used concurrently: NA.The patient was hospitalized. Although Bioclavid demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as neck pain, may still occur.

Hepatotoxicity, Hepatic Necrosis, Jaundice
This Hepatotoxicity, Hepatic Necrosis, Jaundice problem was reported by a consumer or non-health professional from DK. A 78-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: lung infection. On Oct 01, 2012 this consumer started treatment with Bioclavid (dosage: 1000 Mg, Tid). The following drugs were being taken at the same time: NA. When commencing Bioclavid, the patient experienced the following unwanted symptoms/side effects:
  • Hepatotoxicity
  • Hepatic Necrosis
  • Jaundice
The 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 hepatotoxicity, may become evident only after a product is in use by the general population.

Chest Pain, Hepatic Enzyme Increased
This is a report of a 61-year-old female patient (weight: NA) from DK. The patient developed the following symptoms/conditions: infection and was treated with Bioclavid (dosage: 2 Df, Qd) starting May 25, 2011. Concurrently used drugs: NA.Soon after that, the consumer experienced the following side effects:
  • Chest Pain
  • Hepatic Enzyme Increased
The patient was hospitalized. This opens a possibility that Bioclavid treatment could cause the above reactions, including chest pain, and some female subjects may be more susceptible.

Alanine Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Dysphagia, Headache, Malaise, Pain
A female patient (weight: NA) from DENMARK with the following symptoms/conditions: disbacteriosis started Bioclavid (ngx) treatment (dosage: 3000 Mg Daily) on Mar 27, 2007. Soon after starting Bioclavid (ngx) treatment, the subject experienced various side effects, including:
  • Alanine Aminotransferase Increased
  • Blood Alkaline Phosphatase Increased
  • Dysphagia
  • Headache
  • Malaise
  • Pain
Concurrently used drugs: NA.The patient was hospitalized. This finding indicates that some female patients could be more vulnerable to Bioclavid (ngx).

Aphthous Stomatitis, Headache, Lip Swelling, Pain, Swelling Face
A 67-year-old female patient from DENMARK (weight: NA) experienced symptoms, such as: respiratory tract infection and was treated with Bioclavid (amoxicillin, Clavulanate)(dosage: 3 Tables, Qd, Oral). The treatment was initiated on Dec 22, 2006. After that a consumer reported the following side effect(s):
  • Aphthous Stomatitis
  • Headache
  • Lip Swelling
  • Pain
  • Swelling Face
Concurrently used drugs, which potentially could have contributed to side effect(s) or affected Bioclavid (amoxicillin, Clavulanate) efficacy:
  • Spiriva
  • Centyl Med Kaliumklorid ( Bendroflumethiazide, Potassium Chloride)
  • Levothyroxine Sodium
  • Seretide (fluticasone Propionate, Salmeterol Xinafoate

Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Cholangitis, Haemoglobin Decreased, Hepatic Pain, Jaundice, Spleen Disorder
In this report, Bioclavid (ngx) (amoxicillin, Clavulanate) was administered for the following condition: NA.A 15-year-old female consumer from SWEDEN (weight: NA) started Bioclavid (ngx) (amoxicillin, Clavulanate) treatment (dosage: 1 G, Qd, Oral) on May 01, 2005.Sometime after starting the treatment, the patient complained of the following side effect(s):
  • Abdominal Pain
  • Alanine Aminotransferase Increased
  • Aspartate Aminotransferase Increased
  • Cholangitis
  • Haemoglobin Decreased
  • Hepatic Pain
  • Jaundice
  • Spleen Disorder
A possible interaction with other drugs could have contributed to this reaction: NA.The patient was hospitalized.Establishing a causal relationship between a specific drug and consumer's side effects is complex, but it is possible that in this report Bioclavid (ngx) (amoxicillin, Clavulanate) treatment could be related to the listed above side effect(s).

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

    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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    Bioclavid Safety Alerts, Active Ingredients, Usage Information

    More About Bioclavid

    Side Effects reported to FDA: 7

    Bioclavid safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 4

    Latest Bioclavid clinical trials