PatientsVille.com Logo

Lipantil Side Effects

PatientsVille

Common Lipantil Side Effects


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

Jaundice (3)
Hepatic Function Abnormal (2)
Renal Impairment (2)
Gamma-glutamyltransferase Increased (2)
Groin Pain (1)
Hepatitis B Antibody Positive (1)
Gingival Bleeding (1)
Blood Creatinine Increased (1)
Blood Alkaline Phosphatase Increased (1)
Hepatomegaly (1)
Blood Urea Increased (1)
Chromaturia (1)
Rash (1)
Muscle Twitching (1)
Mouth Haemorrhage (1)
Myalgia (1)
Nasal Discomfort (1)
Rectal Haemorrhage (1)
Psoriasis (1)
Influenza Like Illness (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.

Lipantil Side Effects Reported to FDA



Lipantil Side Effect Report#9282115
Psoriasis
This is a report of a 68-year-old female patient (weight: NA) from IE, suffering from the following health symptoms/conditions: myocardial ischaemia, who was treated with Lipantil (dosage: NA, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Psoriasis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Lipantil treatment in female patients, resulting in Psoriasis side effect.
Lipantil Side Effect Report#8146890-0
Muscle Twitching, Groin Pain, Myalgia
This report suggests a potential Lipantil Forte Muscle Twitching side effect(s) that can have serious consequences. A male patient (weight: NA) from Ireland was diagnosed with the following symptoms/conditions: lipids and used Lipantil Forte (dosage: NA) starting
Jan 03, 2012. After starting Lipantil Forte the patient began experiencing various side effects, including: Muscle Twitching, Groin Pain, MyalgiaAdditional drugs used concurrently: NA. Although Lipantil Forte demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Muscle Twitching, may still occur.
Lipantil Side Effect Report#4986868-9
Alanine Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Gingival Bleeding, Influenza Like Illness, Mouth Haemorrhage, Nasal Discomfort, Rash, Rectal Haemorrhage, Tongue Haemorrhage
This Alanine Aminotransferase Increased problem was reported by a health professional from France. A 60-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypercholesterolaemia. On
Feb 04, 2005 this consumer started treatment with Lipantil Micro Capsule (dosage: NA). The following drugs were being taken at the same time:
  • Acetylsalicylic Acid Srt
  • Metoprolol
  • Ramipril
When using Lipantil Micro Capsule, the patient experienced the following unwanted symptoms/side effects: Alanine Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Gingival Bleeding, Influenza Like Illness, Mouth Haemorrhage, Nasal Discomfort, Rash, Rectal Haemorrhage, Tongue HaemorrhageAlthough 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.
Lipantil Side Effect Report#4631067-3
Gamma-glutamyltransferase Increased, Hepatic Function Abnormal, Jaundice
This Gamma-glutamyltransferase Increased side effect was reported by a consumer or non-health professional from . A 62-year-old male patient (weight:NA) experienced the following symptoms/conditions: hyperlipidaemia.The patient was prescribed Lipantil Capsules (drug dosage: NA), which was initiated on
Apr 30, 2003. Concurrently used drugs:
  • Benidipine Hydrochloride
  • Allopurinol
.After starting to take Lipantil Capsules the consumer reported adverse symptoms, such as: Gamma-glutamyltransferase Increased, Hepatic Function Abnormal, JaundiceThese side effects may potentially be related to Lipantil Capsules.
Lipantil Side Effect Report#4593077-4
Gamma-glutamyltransferase Increased, Jaundice
This is a report of a 62-year-old male patient (weight: NA) from , suffering from the following health symptoms/conditions: hyperlipidaemia, who was treated with Lipantil Capsules (dosage: NA, start time:
Apr 01, 2003), combined with:
  • Benidipine Hydrochloride
  • Allopurinol
and developed a serious reaction and side effect(s): Gamma-glutamyltransferase Increased, Jaundice after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Lipantil Capsules treatment in male patients, resulting in Gamma-glutamyltransferase Increased side effect.
Lipantil Side Effect Report#4583153-4
Blood Creatinine Increased, Blood Urea Increased, Renal Impairment
This report suggests a potential Lipantil Blood Creatinine Increased side effect(s) that can have serious consequences. A 56-year-old male patient (weight: NA) from was diagnosed with the following symptoms/conditions: hyperlipidaemia and used Lipantil (dosage: NA) starting
Apr 26, 2004. After starting Lipantil the patient began experiencing various side effects, including: Blood Creatinine Increased, Blood Urea Increased, Renal ImpairmentAdditional drugs used concurrently:
  • Telmisartan
  • Allopurinol
Although Lipantil demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blood Creatinine Increased, may still occur.
Lipantil Side Effect Report#4570433-1
Renal Impairment
This Renal Impairment problem was reported by a consumer or non-health professional from . A 56-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: hyperlipidaemia. On
May 01, 2004 this consumer started treatment with Lipantil (dosage: NA). The following drugs were being taken at the same time:
  • Telmisartan
  • Allopurinol
When using Lipantil, the patient experienced the following unwanted symptoms/side effects: Renal ImpairmentAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Renal Impairment, may become evident only after a product is in use by the general population.
Lipantil Side Effect Report#4551872-1
Chromaturia, Hepatic Function Abnormal, Hepatitis B Antibody Positive, Hepatomegaly, Jaundice
This Chromaturia side effect was reported by a consumer or non-health professional from . A 78-year-old male patient (weight:NA) experienced the following symptoms/conditions: hyperlipidaemia.The patient was prescribed Lipantil (drug dosage: NA), which was initiated on
Jul 01, 2001. Concurrently used drugs:
  • Nitrendipine
.After starting to take Lipantil the consumer reported adverse symptoms, such as: Chromaturia, Hepatic Function Abnormal, Hepatitis B Antibody Positive, Hepatomegaly, JaundiceThese side effects may potentially be related to Lipantil. The patient was hospitalized.



The appearance of Lipantil 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.

300x250 Start Your Diet Today
These healthy diet meal plans are based on the science of what your body needs to lose fat and maintain a lifetime commitment to health. With bistroMD you will enjoy delicious recipes prepared with the right ingredients so that you can learn how to lose weight the healthy way and also rediscover the enjoyment of eating.

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.

    Lipantil 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.

    Discuss Lipantil Side Effects

    Did You Have a Lipantil Side Effect?

    Yes, Severe
    Yes, Moderate
    Yes, Minor
    No

    How Effective is Lipantil for You?

    Exceeded Expectations
    Effective
    Somewhat Effective
    Not Effective

    Lipantil Safety Alerts, Active Ingredients, Usage Information

    More About Lipantil

    Side Effects reported to FDA: 8

    Lipantil safety alerts: No

    Reported hospitalizations: 1

    Latest Lipantil clinical trials

    Lipantil Reviews

    No reviews, be a first to report a side effect via side effect reporting form