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.

Lonarid Side Effects Reported to FDA

Lonarid Side Effect Report#8155544-6
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 health 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): Condition Aggravated, Infection, Chronic Obstructive Pulmonary Disease, Pleuritic Pain, Cardiac Arrest, Infarction 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.
Lonarid Side Effect Report#7867839-1
Thrombocytopenia, Incision Site Haemorrhage
This report suggests a potential Lonarid Thrombocytopenia 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. After starting Lonarid the patient began experiencing various side effects, including: Thrombocytopenia, Incision Site HaemorrhageAdditional 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.
Lonarid Side Effect Report#7629452-0
Stevens-johnson Syndrome, Toxic Epidermal Necrolysis
This Stevens-johnson Syndrome 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 using Lonarid-n (solpadeine /00154101/), the patient experienced the following unwanted symptoms/side effects: Stevens-johnson Syndrome, Toxic Epidermal NecrolysisAlthough 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.
Lonarid Side Effect Report#4983162-7
Amnesia, Body Temperature Decreased, Diarrhoea, Miosis, Post Procedural Vomiting, Suicide Attempt, Tachycardia
This Amnesia side effect was reported by a health professional from Germany. A 28-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Lonarid (drug dosage: 20 Anz Po), which was initiated on 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)
.After starting to take Lonarid the consumer reported adverse symptoms, such as: Amnesia, Body Temperature Decreased, Diarrhoea, Miosis, Post Procedural Vomiting, Suicide Attempt, TachycardiaThese side effects may potentially be related to Lonarid. The patient was hospitalized.

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.

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What are common Lonarid Side Effects for Women?

Women Side EffectsReports
Incision Site Haemorrhage 1
Stevens-johnson Syndrome 1
Thrombocytopenia 1
Toxic Epidermal Necrolysis 1

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.

    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.

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    Discuss Lonarid Side Effects

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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

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