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Marevan Side Effects

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Common Marevan Side Effects


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

International Normalised Ratio Increased (2)
Cardiac Arrest (2)
Haemoglobin Decreased (2)
Diplopia (1)
Unresponsive To Stimuli (1)
Diabetes Mellitus Inadequate Control (1)
American Trypanosomiasis (1)
Oesophagitis (1)
Nephropathy (1)
White Blood Cell Count Increased (1)
Cold Sweat (1)
Haematemesis (1)
Muscular Weakness (1)
Acute Hepatic Failure (1)
Duodenal Ulcer Haemorrhage (1)
Melaena (1)
Loss Of Consciousness (1)
Gastrointestinal Haemorrhage (1)
Heart Rate Increased (1)
Feeling Abnormal (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.

Marevan Side Effects Reported to FDA



Marevan Side Effect Report#8213151-0
American Trypanosomiasis, Cardiac Arrest
This is a report of a 82-year-old female patient (weight: NA) from Brazil, suffering from the following health symptoms/conditions: NA, who was treated with Marevan ^nycomed^ (dosage: Unk, start time: NS), combined with:
  • Xalatan (Unk)
  • Isordil (Unk)
  • Omeprazole (Unk)
and developed a serious reaction and side effect(s): American Trypanosomiasis, Cardiac Arrest after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Marevan ^nycomed^ treatment in female patients, resulting in American Trypanosomiasis side effect.
Marevan Side Effect Report#8125544-0
Unresponsive To Stimuli, Muscular Weakness, Sedation
This report suggests a potential Marevan ^nycomed^ Unresponsive To Stimuli side effect(s) that can have serious consequences. A 85-year-old female patient (weight: NA) from Norway was diagnosed with the following symptoms/conditions: NA and used Marevan ^nycomed^ (dosage: As Per Schedule) starting
Oct 07, 2011. After starting Marevan ^nycomed^ the patient began experiencing various side effects, including: Unresponsive To Stimuli, Muscular Weakness, SedationAdditional drugs used concurrently:
  • Bumetanide (2 Mg, 1x/day)
  • Digitoxin Inj (50 Ug 4 Days A Week)
  • Atacand (4 Mg, 1x/day)
  • Symbicort (160/45, 2x/day)
  • Lyrica
  • Spironolactone (12.5 Mg, 1x/day)
  • Metoprolol Succinate (100 Mg, 1x/day)
  • Allopur (100 Mg, 2x/day)
Although Marevan ^nycomed^ demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Unresponsive To Stimuli, may still occur.
Marevan Side Effect Report#7784140-5
Acute Hepatic Failure, Sepsis, Nephropathy
This Acute Hepatic Failure problem was reported by a health professional from Denmark. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Aug 28, 2010 this consumer started treatment with Marevan ^nycomed^ (dosage: NA). The following drugs were being taken at the same time:
  • Dexamethasone
  • Revlimid (25 Milligram)
When using Marevan ^nycomed^, the patient experienced the following unwanted symptoms/side effects: Acute Hepatic Failure, Sepsis, NephropathyThe 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 Acute Hepatic Failure, may become evident only after a product is in use by the general population.
Marevan Side Effect Report#7406117-1
Syncope
This Syncope side effect was reported by a consumer or non-health professional from Brazil. A 92-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Marevan ^nycomed^ (drug dosage: Unk), which was initiated on
Mar 01, 2008. Concurrently used drugs:
  • Diamicron (Unk)
  • Frontal (Unk)
  • Frontal
  • Atenolol (Unk)
  • Detrusitol La (4 Mg, 1x/day (at Nigth))
  • Sinergen (Unk)
  • Detrusitol La
  • Furosemide (Unk)
.After starting to take Marevan ^nycomed^ the consumer reported adverse symptoms, such as: SyncopeThese side effects may potentially be related to Marevan ^nycomed^.
Marevan Side Effect Report#7292451-5
Diplopia
This is a report of a 79-year-old female patient (weight: NA) from Finland, suffering from the following health symptoms/conditions: NA, who was treated with Marevan ^orion^ (dosage: Unk, start time:
Nov 26, 2010), combined with:
  • Seloken (95 Mg, Unk)
  • Coversyl (10 Mg, Unk)
  • Revatio (20 Mg, 3x/day)
and developed a serious reaction and side effect(s): Diplopia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Marevan ^orion^ treatment in female patients, resulting in Diplopia side effect.
Marevan Side Effect Report#7277947-4
Gastric Ulcer Haemorrhage, Gastrointestinal Haemorrhage, Duodenal Ulcer Haemorrhage, Cardiac Arrest
This report suggests a potential Marevan Gastric Ulcer Haemorrhage side effect(s) that can have serious consequences. A 87-year-old male patient (weight: NA) from was diagnosed with the following symptoms/conditions: atrial fibrillation and used Marevan (dosage: 5 Mg) starting
Jan 20, 2010. After starting Marevan the patient began experiencing various side effects, including: Gastric Ulcer Haemorrhage, Gastrointestinal Haemorrhage, Duodenal Ulcer Haemorrhage, Cardiac ArrestAdditional drugs used concurrently:
  • Pradaxa (110 Mg)
Although Marevan demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Gastric Ulcer Haemorrhage, may still occur.
Marevan Side Effect Report#5105429-4
Cold Sweat, Feeling Abnormal, Haemoglobin Decreased, Heart Rate Increased, International Normalised Ratio Increased, Melaena, Pulse Pressure Increased, White Blood Cell Count Increased
This Cold Sweat problem was reported by a health professional from Norway. A 77-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: cardiac valve prosthesis user,depression,anaemia,pain. On
Jul 13, 2006 this consumer started treatment with Marevan (dosage: 5 Mg/day). The following drugs were being taken at the same time:
  • Escitalopram Oxalate (20 Mg/day)
  • Nycoplus Ferro (100 Mg, Bid)
  • Pinex (1 G, Qid)
  • Oxynorm (5 Mg X 2 To 4 Times)
  • Isoptin (120 Mg, Qd)
  • Zopiclone (7.5 Mg, Qd)
  • Voltaren (50 Mg, Tid)
When using Marevan, the patient experienced the following unwanted symptoms/side effects: Cold Sweat, Feeling Abnormal, Haemoglobin Decreased, Heart Rate Increased, International Normalised Ratio Increased, Melaena, Pulse Pressure Increased, White Blood Cell Count IncreasedAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Cold Sweat, may become evident only after a product is in use by the general population.
Marevan Side Effect Report#4937205-7
Loss Of Consciousness, Pancreatitis
This Loss Of Consciousness side effect was reported by a consumer or non-health professional from Finland. A 50-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Marevan (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Bisoprolol
  • Canef (licensed To Astra) (40 Mg, Qd)
.After starting to take Marevan the consumer reported adverse symptoms, such as: Loss Of Consciousness, PancreatitisThese side effects may potentially be related to Marevan. The patient was hospitalized.
Marevan Side Effect Report#4620214-5
Diabetes Mellitus Inadequate Control, Haematemesis, Haemoglobin Decreased, International Normalised Ratio Increased, Oesophagitis
This is a report of a 76-year-old male patient (weight: NA) from , suffering from the following health symptoms/conditions: mitral valve disease, who was treated with Marevan (dosage: NA, start time: NS), combined with:
  • Rosuvastatin
  • Minidiab
  • Orabet
  • Magnyl
  • Digoxin
  • Spiron
  • Cozaar
  • Selozok
and developed a serious reaction and side effect(s): Diabetes Mellitus Inadequate Control, Haematemesis, Haemoglobin Decreased, International Normalised Ratio Increased, Oesophagitis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Marevan treatment in male patients, resulting in Diabetes Mellitus Inadequate Control side effect. The patient was hospitalized.


The appearance of Marevan 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.

    Marevan 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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    Marevan Safety Alerts, Active Ingredients, Usage Information

    More About Marevan

    Side Effects reported to FDA: 9

    Marevan safety alerts: No

    Reported deaths: 2

    Reported hospitalizations: 2

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