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Bioclavid Side Effects

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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.

Bioclavid Side Effects Reported to FDA



Bioclavid Side Effect Report#9155815
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 health 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): Hepatitis, Liver Disorder, Pyrexia, Malaise, Confusional State 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.
Bioclavid Side Effect Report#9101895
Neck Pain, Diplegia, Convulsion, Rash
This report suggests a potential Bioclavid Neck Pain 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. After starting Bioclavid the patient began experiencing various side effects, including: Neck Pain, Diplegia, Convulsion, RashAdditional 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.
Bioclavid Side Effect Report#9031011
Hepatotoxicity, Hepatic Necrosis, Jaundice
This Hepatotoxicity 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 using Bioclavid, the patient experienced the following unwanted symptoms/side effects: Hepatotoxicity, Hepatic Necrosis, JaundiceThe 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.
Bioclavid Side Effect Report#8967162
Chest Pain, Hepatic Enzyme Increased
This Chest Pain side effect was reported by a health professional from DK. A 61-year-old female patient (weight:NA) experienced the following symptoms/conditions: infection.The patient was prescribed Bioclavid (drug dosage: 2 Df, Qd), which was initiated on
May 25, 2011. Concurrently used drugs: NA..After starting to take Bioclavid the consumer reported adverse symptoms, such as: Chest Pain, Hepatic Enzyme IncreasedThese side effects may potentially be related to Bioclavid. The patient was hospitalized.
Bioclavid Side Effect Report#6664393-7
Alanine Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Dysphagia, Headache, Malaise, Pain
This is a report of a female patient (weight: NA) from Denmark, suffering from the following health symptoms/conditions: disbacteriosis, who was treated with Bioclavid (ngx) (dosage: 3000 Mg Daily, start time:
Mar 27, 2007), combined with: NA. and developed a serious reaction and side effect(s): Alanine Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Dysphagia, Headache, Malaise, Pain after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Bioclavid (ngx) treatment in female patients, resulting in Alanine Aminotransferase Increased side effect. The patient was hospitalized.
Bioclavid Side Effect Report#5209687-7
Aphthous Stomatitis, Headache, Lip Swelling, Pain, Swelling Face
This report suggests a potential Bioclavid (amoxicillin, Clavulanate) Aphthous Stomatitis side effect(s) that can have serious consequences. A 67-year-old female patient (weight: NA) from Denmark was diagnosed with the following symptoms/conditions: respiratory tract infection and used Bioclavid (amoxicillin, Clavulanate) (dosage: 3 Tables, Qd, Oral) starting
Dec 22, 2006. After starting Bioclavid (amoxicillin, Clavulanate) the patient began experiencing various side effects, including: Aphthous Stomatitis, Headache, Lip Swelling, Pain, Swelling FaceAdditional drugs used concurrently:
  • Spiriva
  • Centyl Med Kaliumklorid ( Bendroflumethiazide, Potassium Chloride)
  • Levothyroxine Sodium
  • Seretide (fluticasone Propionate, Salmeterol Xinafoate
Although Bioclavid (amoxicillin, Clavulanate) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Aphthous Stomatitis, may still occur.
Bioclavid Side Effect Report#4777922-5
Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Cholangitis, Haemoglobin Decreased, Hepatic Pain, Jaundice, Spleen Disorder
This Abdominal Pain problem was reported by a consumer or non-health professional from Sweden. A 15-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
May 01, 2005 this consumer started treatment with Bioclavid (ngx) (amoxicillin, Clavulanate) (dosage: 1 G, Qd, Oral). The following drugs were being taken at the same time: NA. When using Bioclavid (ngx) (amoxicillin, Clavulanate), the patient experienced the following unwanted symptoms/side effects: Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Cholangitis, Haemoglobin Decreased, Hepatic Pain, Jaundice, Spleen DisorderThe 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.



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.


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.

    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.

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    More About Bioclavid

    Side Effects reported to FDA: 7

    Bioclavid safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 4

    Latest Bioclavid clinical trials