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Piascledine Side Effects

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Common Piascledine Side Effects


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

Tachycardia (1)
Syncope (1)
Sudden Death (1)
Renal Failure (1)
Thrombophlebitis (1)
Torticollis (1)
Neutropenia (1)
Oedema Peripheral (1)
Tremor (1)
Pulmonary Embolism (1)
Porphyrins Urine Increased (1)
Pallor (1)
Osteoarthritis (1)
Orthostatic Hypotension (1)
Palpitations (1)
Pancytopenia (1)
Porphyrins Stool Increased (1)
Porphyrin Metabolism Disorder (1)
Porphyria Non-acute (1)
Anaphylactic Shock (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.

Piascledine Side Effects Reported to FDA



Piascledine Side Effect Report#8303079-X
Delusion
This is a report of a 78-year-old female patient (weight: NA) from France, suffering from the following health symptoms/conditions: hypertension,bipolar disorder, who was treated with Piascledine (dosage: Avocado Oil Unsaponifiables And Soya Oil Unsaponifiables, start time:
Jul 01, 2011), combined with:
  • Tegretol
  • Abilify (10 Mg Morning And 20 Mg Evening)
  • Levothyroxine Sodium (Levothyrox (levothyroxin Sodium) 75 Mg Morning)
  • Fenofibrate
  • Cozaar
and developed a serious reaction and side effect(s): Delusion after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Piascledine treatment in female patients, resulting in Delusion side effect.
Piascledine Side Effect Report#8134123-0
Palpitations, Tachycardia, Chills, Infusion Related Reaction
This report suggests a potential Piascledine /01305801/ Palpitations side effect(s) that can have serious consequences. A female patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Piascledine /01305801/ (dosage: 1 G, 1x/day:qd) starting
Dec 20, 2011. After starting Piascledine /01305801/ the patient began experiencing various side effects, including: Palpitations, Tachycardia, Chills, Infusion Related ReactionAdditional drugs used concurrently:
  • Caltrate /00751519/ (600 Mg, 1x/day:qd)
  • Augmentin '125'
  • Vpriv
  • Birodogyl
The patient was hospitalized. Although Piascledine /01305801/ demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Palpitations, may still occur.
Piascledine Side Effect Report#8118240-7
Torticollis, Arthralgia, Oedema Peripheral, Gastrointestinal Haemorrhage, Muscle Contracture
This Torticollis problem was reported by a health professional from Denmark. A 72-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Nov 16, 2011 this consumer started treatment with Piascledine (avocado Oil, Soya Oil) (300 Milligram, Tablets) (avocado (dosage: NA). The following drugs were being taken at the same time:
  • Topalgic (tramadol Hydrochloride) (200 Milligram, Tablets) (tramadol H
  • Lexomil (bromazepam) (tablets) (bromazepam)
  • Escitalopram (1 Dosage Form (1 Dosage Forms, 1 In 1 D), Oral)
When using Piascledine (avocado Oil, Soya Oil) (300 Milligram, Tablets) (avocado, the patient experienced the following unwanted symptoms/side effects: Torticollis, Arthralgia, Oedema Peripheral, Gastrointestinal Haemorrhage, Muscle ContractureAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Torticollis, may become evident only after a product is in use by the general population.
Piascledine Side Effect Report#7974230-6
Asthenia, Pancytopenia, Weight Decreased, Anaphylactic Shock, Castleman's Disease
This Asthenia side effect was reported by a physician from France. A 45-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Piascledine (drug dosage: NA), which was initiated on
Aug 11, 2010. Concurrently used drugs:
  • Norvir
  • Sustiva
  • Prezista
  • Nevirapine
  • Isentress
  • Isentress
  • Viread
  • Reyataz
.After starting to take Piascledine the consumer reported adverse symptoms, such as: Asthenia, Pancytopenia, Weight Decreased, Anaphylactic Shock, Castleman's DiseaseThese side effects may potentially be related to Piascledine. The patient was hospitalized.
Piascledine Side Effect Report#7902413-X
Thrombophlebitis, Chest Pain, Pulmonary Embolism
This is a report of a female patient (weight: NA) from France, suffering from the following health symptoms/conditions: NA, who was treated with Piascledine (dosage: NA, start time: NS), combined with:
  • Fenofibrate
  • Pradaxa
  • Valsartan And Hydrochlorothiazide
  • Pradaxa (150 Mg)
and developed a serious reaction and side effect(s): Thrombophlebitis, Chest Pain, Pulmonary Embolism after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Piascledine treatment in female patients, resulting in Thrombophlebitis side effect. The patient was hospitalized.
Piascledine Side Effect Report#7485580-4
Tremor
This report suggests a potential Piascledine Tremor side effect(s) that can have serious consequences. A male patient (weight: NA) from United Kingdom was diagnosed with the following symptoms/conditions: NA and used Piascledine (dosage: Unk) starting
Nov 15, 2010. After starting Piascledine the patient began experiencing various side effects, including: TremorAdditional drugs used concurrently:
  • Ondansertron Hydrochloride (Unk)
  • Bricanyl (Unk)
  • Ceris (Unk)
  • Bendamustine (300 Mg, Q4w)
  • Pravastatin Sodium (Unk)
  • Atrovent (Unk)
  • Diltiazem (Unk)
  • Rituximab (825 Mg, Q4w)
The patient was hospitalized. Although Piascledine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Tremor, may still occur.
Piascledine Side Effect Report#7476384-7
Neutropenia
This Neutropenia problem was reported by a physician from France. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jan 01, 2008 this consumer started treatment with Piascledine (dosage: NA). The following drugs were being taken at the same time:
  • Lapatinib (1250mg Per Day)
  • Allopurinol
  • Docetaxel
  • Levothyroxine Sodium
  • Imovane
When using Piascledine, the patient experienced the following unwanted symptoms/side effects: NeutropeniaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Neutropenia, may become evident only after a product is in use by the general population.
Piascledine Side Effect Report#7246881-8
Joint Injury, Osteoarthritis, Nausea
This Joint Injury side effect was reported by a physician from France. A 67-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Piascledine /00809501/ (drug dosage: 1 Dosage, Daily (1/d)), which was initiated on
Mar 23, 2010. Concurrently used drugs:
  • Forteo (20 Ug, Daily (1/d))
.After starting to take Piascledine /00809501/ the consumer reported adverse symptoms, such as: Joint Injury, Osteoarthritis, NauseaThese side effects may potentially be related to Piascledine /00809501/. The patient was hospitalized.
Piascledine Side Effect Report#5226543-9
Iron Metabolism Disorder, Porphyria Non-acute, Porphyrin Metabolism Disorder, Porphyrins Stool Increased, Porphyrins Urine Increased
This is a report of a male patient (weight: NA) from France, suffering from the following health symptoms/conditions: NA, who was treated with Piascledine (dosage: NA, start time:
Jun 29, 2006), combined with:
  • Hysaar
  • Levothyroxine Sodium
  • Plavix
and developed a serious reaction and side effect(s): Iron Metabolism Disorder, Porphyria Non-acute, Porphyrin Metabolism Disorder, Porphyrins Stool Increased, Porphyrins Urine Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Piascledine treatment in male patients, resulting in Iron Metabolism Disorder side effect.
Piascledine Side Effect Report#5083666-5
Cardio-respiratory Arrest
This report suggests a potential Piascledine Cardio-respiratory Arrest side effect(s) that can have serious consequences. A 61-year-old male patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Piascledine (dosage: Unk) starting
Jun 03, 2006. After starting Piascledine the patient began experiencing various side effects, including: Cardio-respiratory ArrestAdditional drugs used concurrently:
  • Tanakan (120 Mg)
  • Risperdal
  • Risperdal
  • Risperdal
  • Rivotril
  • Risperdal Consta Lp (1 Vial Nos Every Two Weeks)
  • Noctamide
  • Stilnox (Unk)
Although Piascledine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Cardio-respiratory Arrest, may still occur.
Piascledine Side Effect Report#4846841-8
Blood Creatinine Increased, Creatinine Renal Clearance Decreased, Discomfort, Faecal Incontinence, Malaise, Orthostatic Hypotension, Pallor, Renal Failure, Syncope
This Blood Creatinine Increased problem was reported by a consumer or non-health professional from France. A 91-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Piascledine (dosage: NA). The following drugs were being taken at the same time:
  • Orocal
  • Tanakan
  • Ditropan
  • Diffu K
  • Briazide (1 Df, Qd)
When using Piascledine, the patient experienced the following unwanted symptoms/side effects: Blood Creatinine Increased, Creatinine Renal Clearance Decreased, Discomfort, Faecal Incontinence, Malaise, Orthostatic Hypotension, Pallor, Renal Failure, SyncopeThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Blood Creatinine Increased, may become evident only after a product is in use by the general population.


The appearance of Piascledine 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.


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.

    Piascledine 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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