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.
Strocain Side Effects Reported to FDA
Strocain Side Effect Report#8448289-6 Acute Abdomen, Sepsis
This is a report of a 62-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: abdominal pain upper, who was treated with Strocain /00130301/ (dosage: 10 Df, 1x/week, start time:
Dec 15, 2006), combined with:
Rhubarb Dry Extract
Foliamin (2 Df, 1x/week)
and developed a serious reaction and side effect(s): Acute Abdomen, Sepsis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Strocain /00130301/ treatment in female patients, resulting in Acute Abdomen side effect. The patient was hospitalized.
Strocain Side Effect Report#8419470-7 Infection, Neuroleptic Malignant Syndrome
This report suggests a potential StrocainInfection side effect(s) that can have serious consequences. A 80-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Strocain (dosage: Unk) starting
Dec 09, 2011. After starting Strocain the patient began experiencing various side effects, including: Infection, Neuroleptic Malignant SyndromeAdditional drugs used concurrently:
Ethyl Icosapentate (Unk)
Lithium Carbonate (Unk)
Zyprexa (10 Mg, Qd)
The patient was hospitalized. Although Strocain demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Infection, may still occur.
Strocain Side Effect Report#7482666-5 Breast Mass
This Breast Mass problem was reported by a pharmacist from Japan. A 62-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Feb 19, 2011 this consumer started treatment with Strocain (dosage: Unk). The following drugs were being taken at the same time:
Lac B (Unk)
Varenicline Tartrate (0.5 Mg, 2x/day)
Varenicline Tartrate (Unk)
When using Strocain, the patient experienced the following unwanted symptoms/side effects: Breast MassAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Breast Mass, may become evident only after a product is in use by the general population.
The appearance of Strocain 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.
Strocain 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.