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.
Lutenyl Side Effects Reported to FDA
Lutenyl Side Effect Report#7861399-7 Erythema Multiforme
This is a report of a 48-year-old female patient (weight: NA) from France, suffering from the following health symptoms/conditions: NA, who was treated with Lutenyl (dosage: Unk, start time:
Jun 26, 2011), combined with:
Ibuprofen (advil) (Unk %, Single)
and developed a serious reaction and side effect(s): Erythema Multiforme after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Lutenyl treatment in female patients, resulting in Erythema Multiforme side effect. The patient was hospitalized.
Lutenyl Side Effect Report#7784850-X Psychomotor Hyperactivity, Hypomania, Haematoma
This report suggests a potential LutenylPsychomotor Hyperactivity side effect(s) that can have serious consequences. A 41-year-old female patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Lutenyl (dosage: Unk) starting
May 10, 2011. After starting Lutenyl the patient began experiencing various side effects, including: Psychomotor Hyperactivity, Hypomania, HaematomaAdditional drugs used concurrently:
Sertraline Hydrochloride (50 Mg, Alternate Day)
Sertraline Hydrochloride (50 Mg, 1x/day)
Although Lutenyl demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Psychomotor Hyperactivity, may still occur.
Lutenyl Side Effect Report#5242547-4 Abortion Induced
This Abortion Induced problem was reported by a physician from France. A 31-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: ill-defined disorder,hypertension. On NS this consumer started treatment with Lutenyl (dosage: NA). The following drugs were being taken at the same time:
Perindopril Erbumine (Daily Dose: 4 Milligram(s))
When using Lutenyl, the patient experienced the following unwanted symptoms/side effects: Abortion InducedAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Abortion Induced, may become evident only after a product is in use by the general population.
The appearance of Lutenyl 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.
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
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:
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.
Lutenyl 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.