Lonarid Side Effects

Common Lonarid Side Effects

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

Condition Aggravated (1)
Diarrhoea (1)
Incision Site Haemorrhage (1)
Chronic Obstructive Pulmonary Disease (1)
Cardiac Arrest (1)
Toxic Epidermal Necrolysis (1)
Body Temperature Decreased (1)
Infarction (1)
Infection (1)
Suicide Attempt (1)
Tachycardia (1)
Thrombocytopenia (1)
Stevens-johnson Syndrome (1)
Post Procedural Vomiting (1)
Miosis (1)
Pleuritic Pain (1)
Amnesia (1)

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.

Lonarid Side Effects Reported to FDA

The following Lonarid 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 Lonarid 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.
Condition Aggravated, Infection, Chronic Obstructive Pulmonary Disease, Pleuritic Pain, Cardiac Arrest, Infarction
This is a report of a 72-year-old male patient (weight: NA) from DENMARK, suffering from the following symptoms/conditions: NA, who was treated with Lonarid (solpadeine) (solpadeine) (dosage: NA, start time: Nov 01, 2011), combined with:
  • Roflumilast (roflumilast) (tablets) (1 Dosage Forms (1 Dosage Forms, 1 In 1 D), Oral)
  • Spiriva (tiotropium Bromide) (inhalant) (tiotropium Bromide)
  • Seretide Diskus (seretide) (inhalant) (seretide)
  • Depon (paracetamol) (paracetamol)
and developed a serious reaction and side effect(s). The consumer presented with:
  • Condition Aggravated
  • Infection
  • Chronic Obstructive Pulmonary Disease
  • Pleuritic Pain
  • Cardiac Arrest
  • Infarction
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Lonarid (solpadeine) (solpadeine) treatment in male patients, resulting in condition aggravated side effect.

Thrombocytopenia, Incision Site Haemorrhage
This report suggests a potential Lonarid Thrombocytopenia, Incision Site Haemorrhage side effect(s) that can have serious consequences. A 74-year-old female patient (weight: NA) from GREECE was diagnosed with the following symptoms/conditions: NA and used Lonarid (dosage: NA) starting Oct 18, 2011. Soon after starting Lonarid the patient began experiencing various side effects, including:
  • Thrombocytopenia
  • Incision Site Haemorrhage
Drugs used concurrently:
  • Zantac
  • Blood And Related Products
  • Rivaroxaban
  • Cefuroxime Sodium
The patient was hospitalized. Although Lonarid demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as thrombocytopenia, may still occur.

Stevens-johnson Syndrome, Toxic Epidermal Necrolysis
This Stevens-johnson Syndrome, Toxic Epidermal Necrolysis problem was reported by a consumer or non-health professional from GREECE. A 37-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On Apr 15, 2011 this consumer started treatment with Lonarid-n (solpadeine /00154101/) (dosage: NA). The following drugs were being taken at the same time:
  • Methylprednisolone (medrol) (methylprednisolone)
  • Omeprazole
  • Phenytoin Sodium Cap (300 Mg, D, Oral)
  • Omniscan (Single Dose, Intravenous)
When commencing Lonarid-n (solpadeine /00154101/), the patient experienced the following unwanted symptoms/side effects:
  • Stevens-johnson Syndrome
  • Toxic Epidermal Necrolysis
Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as stevens-johnson syndrome, may become evident only after a product is in use by the general population.

Amnesia, Body Temperature Decreased, Diarrhoea, Miosis, Post Procedural Vomiting, Suicide Attempt, Tachycardia
This is a report of a 28-year-old male patient (weight: NA) from GERMANY. The patient developed the following symptoms/conditions: NA and was treated with Lonarid (dosage: 20 Anz Po) starting NS. Concurrently used drugs:
  • Optalidon (ibuprofen) (30 Anz (nr), Po)
  • Mefenamic Acid (70 Anz (500 Mg), Po)
  • Zopiclon (zopiclone) (150 Mg (7.5 Mg) Po)
Soon after that, the consumer experienced the following side effects:
  • Amnesia
  • Body Temperature Decreased
  • Diarrhoea
  • Miosis
  • Post Procedural Vomiting
  • Suicide Attempt
  • Tachycardia
The patient was hospitalized. This opens a possibility that Lonarid treatment could cause the above reactions, including amnesia, and some male subjects may be more susceptible.

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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    Lonarid Safety Alerts, Active Ingredients, Usage Information

    More About Lonarid

    Side Effects reported to FDA: 4

    Lonarid safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 2

    Latest Lonarid clinical trials

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