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Magnex Side Effects

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Common Magnex Side Effects


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

Platelet Count Decreased (8)
Thrombocytopenia (7)
Prothrombin Time Prolonged (5)
Anaphylactic Shock (4)
International Normalised Ratio Increased (4)
Renal Failure Acute (3)
Gastrointestinal Haemorrhage (3)
Sepsis (3)
Septic Shock (3)
Rash (3)
Haemorrhage Urinary Tract (3)
Grand Mal Convulsion (3)
Death (3)
Post Procedural Haemorrhage (2)
Respiratory Arrest (2)
Haematuria (2)
Abdominal Abscess (2)
Tracheal Haemorrhage (2)
Cardiac Arrest (2)
Cerebral Haemorrhage (2)

➢ 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.

Magnex Side Effects Reported to FDA



Magnex Side Effect Report#7081919-2
Anaphylactic Shock
This is a report of a 34-year-old female patient (weight: NA) from India, suffering from the following health symptoms/conditions: infection, who was treated with Magnex (dosage: 1 G, Unk, start time:
Oct 14, 2010), combined with: NA. and developed a serious reaction and side effect(s): Anaphylactic Shock after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Magnex treatment in female patients, resulting in Anaphylactic Shock side effect.
Magnex Side Effect Report#7056446-9
Anaphylactic Shock
This report suggests a potential Magnex Anaphylactic Shock side effect(s) that can have serious consequences. A 34-year-old female patient (weight: NA) from India was diagnosed with the following symptoms/conditions: infection and used Magnex (dosage: Unk) starting NS. After starting Magnex the patient began experiencing various side effects, including: Anaphylactic ShockAdditional drugs used concurrently: NA. Although Magnex demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Anaphylactic Shock, may still occur.
Magnex Side Effect Report#7056429-9
This Death problem was reported by a physician from India. A 52-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: sepsis. On NS this consumer started treatment with Magnex (dosage: 1.5 G, 3x/day). The following drugs were being taken at the same time:
  • Amikacin (1 G, 1x/day)
When using Magnex, the patient experienced the following unwanted symptoms/side effects:Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Death, may become evident only after a product is in use by the general population.
Magnex Side Effect Report#7054180-2
This Death side effect was reported by a physician from India. A 85-year-old male patient (weight:NA) experienced the following symptoms/conditions: pneumonia.The patient was prescribed Magnex (drug dosage: 3 G, 2x/day), which was initiated on NS. Concurrently used drugs:
  • Metrogyl (500 Mg, 3x/day)
.After starting to take Magnex the consumer reported adverse symptoms, such as: These side effects may potentially be related to Magnex.
Magnex Side Effect Report#7039903-0
Stevens-johnson Syndrome
This is a report of a 57-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: NA, who was treated with Magnex (dosage: 3 G, 1x/day, start time:
Aug 30, 2010), combined with:
  • Amlodipine (Unk)
  • Atenolol (Unk)
  • Minipress Xl (Unk)
  • Shelcal (Unk)
  • Atorvastatin (Unk)
  • Iron (Unk)
  • Folate (Unk)
  • Pantoprazole (Unk)
and developed a serious reaction and side effect(s): Stevens-johnson Syndrome after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Magnex treatment in male patients, resulting in Stevens-johnson Syndrome side effect. The patient was hospitalized.
Magnex Side Effect Report#7038067-7
Blood Glucose Increased, Pneumonia, Stevens-johnson Syndrome
This report suggests a potential Magnex Blood Glucose Increased side effect(s) that can have serious consequences. A 67-year-old male patient (weight: NA) from India was diagnosed with the following symptoms/conditions: NA and used Magnex (dosage: 3 G, 1x/day) starting
Aug 28, 2010. After starting Magnex the patient began experiencing various side effects, including: Blood Glucose Increased, Pneumonia, Stevens-johnson SyndromeAdditional drugs used concurrently:
  • Atorvastatin
  • Mixtard Human 70/30 (40 Iu)
  • Ranitidine
  • Amlodipine
  • Clopidogrel
  • Erythropoietin
Although Magnex demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blood Glucose Increased, may still occur.
Magnex Side Effect Report#6930154-4
Acute Respiratory Distress Syndrome, Atrial Fibrillation, Chest Discomfort, Decubitus Ulcer, Dyspnoea, Hyperhidrosis, Lower Respiratory Tract Infection, Pleural Effusion, Sepsis
This Acute Respiratory Distress Syndrome problem was reported by a physician from India. A 69-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Oct 20, 2008 this consumer started treatment with Magnex (dosage: 1 G, 2x/day). The following drugs were being taken at the same time: NA. When using Magnex, the patient experienced the following unwanted symptoms/side effects: Acute Respiratory Distress Syndrome, Atrial Fibrillation, Chest Discomfort, Decubitus Ulcer, Dyspnoea, Hyperhidrosis, Lower Respiratory Tract Infection, Pleural Effusion, SepsisThe 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 Respiratory Distress Syndrome, may become evident only after a product is in use by the general population.
Magnex Side Effect Report#6924940-4
Full Blood Count Decreased
This Full Blood Count Decreased side effect was reported by a physician from India. A 52-year-old female patient (weight:NA) experienced the following symptoms/conditions: sepsis.The patient was prescribed Magnex (drug dosage: Unk), which was initiated on NS. Concurrently used drugs: NA..After starting to take Magnex the consumer reported adverse symptoms, such as: Full Blood Count DecreasedThese side effects may potentially be related to Magnex.
Magnex Side Effect Report#6657412-5
Thrombocytopenia
This is a report of a 45-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: surgery, who was treated with Magnex (dosage: 1 G, 2x/day, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Thrombocytopenia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Magnex treatment in male patients, resulting in Thrombocytopenia side effect.
Magnex Side Effect Report#6544858-9
Pancytopenia
This report suggests a potential Magnex Pancytopenia side effect(s) that can have serious consequences. A 42-year-old male patient (weight: NA) from India was diagnosed with the following symptoms/conditions: head injury,epilepsy and used Magnex (dosage: 2 G, 3x/day) starting
Jan 04, 2010. After starting Magnex the patient began experiencing various side effects, including: PancytopeniaAdditional drugs used concurrently:
  • Phenytoin (Unk)
Although Magnex demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Pancytopenia, may still occur.
Magnex Side Effect Report#6398720-5
Rash
This Rash problem was reported by a physician from India. A 12-year-old patient (weight: NA) was diagnosed with the following symptoms/conditions: wound infection. On
Jun 03, 2009 this consumer started treatment with Magnex (dosage: 1.5 G, 2x/day). The following drugs were being taken at the same time:
  • Vancomycin
When using Magnex, the patient experienced the following unwanted symptoms/side effects: RashAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Rash, may become evident only after a product is in use by the general population.
Magnex Side Effect Report#6374439-1
Cerebral Haemorrhage, Gastrointestinal Haemorrhage, Haematuria, Thrombocytopenia
This Cerebral Haemorrhage side effect was reported by a consumer or non-health professional from India. A 28-year-old patient (weight:NA) experienced the following symptoms/conditions: sepsis,multiple injuries.The patient was prescribed Magnex (drug dosage: 2 G, 2x/day), which was initiated on
Aug 23, 2009. Concurrently used drugs: NA..After starting to take Magnex the consumer reported adverse symptoms, such as: Cerebral Haemorrhage, Gastrointestinal Haemorrhage, Haematuria, ThrombocytopeniaThese side effects may potentially be related to Magnex.
Magnex Side Effect Report#6348851-0
Thrombocytopenia
This is a report of a 28-year-old patient (weight: NA) from India, suffering from the following health symptoms/conditions: head injury, who was treated with Magnex (dosage: 2 G, 2x/day, start time:
Aug 23, 2009), combined with:
  • Gentamicin
and developed a serious reaction and side effect(s): Thrombocytopenia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Magnex treatment in patients, resulting in Thrombocytopenia side effect.
Magnex Side Effect Report#6249362-3
Rash
This report suggests a potential Magnex Rash side effect(s) that can have serious consequences. A 12-year-old patient (weight: NA) from India was diagnosed with the following symptoms/conditions: wound infection and used Magnex (dosage: 1.5 G, 2x/day) starting
Jun 03, 2009. After starting Magnex the patient began experiencing various side effects, including: RashAdditional drugs used concurrently:
  • Vancomycin
Although Magnex demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Rash, may still occur.
Magnex Side Effect Report#6228787-6
Rash
This Rash problem was reported by a physician from India. A 12-year-old patient (weight: NA) was diagnosed with the following symptoms/conditions: wound infection. On
Jun 03, 2009 this consumer started treatment with Magnex (dosage: 1.5 G, 2x/day). The following drugs were being taken at the same time:
  • Vancomycin
When using Magnex, the patient experienced the following unwanted symptoms/side effects: RashAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Rash, may become evident only after a product is in use by the general population.
Magnex Side Effect Report#5949046-2
Blood Pressure Decreased, Pyrexia
This Blood Pressure Decreased side effect was reported by a physician from India. A 28-year-old male patient (weight:NA) experienced the following symptoms/conditions: acute respiratory distress syndrome.The patient was prescribed Magnex (drug dosage: NA), which was initiated on
Sep 23, 2008. Concurrently used drugs: NA..After starting to take Magnex the consumer reported adverse symptoms, such as: Blood Pressure Decreased, PyrexiaThese side effects may potentially be related to Magnex. The patient was hospitalized.
Magnex Side Effect Report#5774424-4
Platelet Count Decreased, Septic Shock
This is a report of a 23-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: peritonitis, who was treated with Magnex (dosage: NA, start time:
May 14, 2008), combined with:
  • Metronidazole
  • Amikacin
  • Vitamin K Tab
and developed a serious reaction and side effect(s): Platelet Count Decreased, Septic Shock after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Magnex treatment in male patients, resulting in Platelet Count Decreased side effect.
Magnex Side Effect Report#5751385-5
Platelet Count Decreased
This report suggests a potential Magnex Platelet Count Decreased side effect(s) that can have serious consequences. A 23-year-old male patient (weight: NA) from India was diagnosed with the following symptoms/conditions: peritonitis and used Magnex (dosage: NA) starting
May 14, 2008. After starting Magnex the patient began experiencing various side effects, including: Platelet Count DecreasedAdditional drugs used concurrently:
  • Metronidazole Hcl
  • Amikacin
  • Vitamin K Tab
Although Magnex demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Platelet Count Decreased, may still occur.
Magnex Side Effect Report#5692206-9
International Normalised Ratio Increased
This International Normalised Ratio Increased problem was reported by a physician from India. A 50-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: lung infection. On NS this consumer started treatment with Magnex (dosage: NA). The following drugs were being taken at the same time:
  • Amikacin
When using Magnex, the patient experienced the following unwanted symptoms/side effects: International Normalised Ratio IncreasedThe 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 International Normalised Ratio Increased, may become evident only after a product is in use by the general population.
Magnex Side Effect Report#5679593-2
International Normalised Ratio Increased
This International Normalised Ratio Increased side effect was reported by a physician from India. A 50-year-old male patient (weight:NA) experienced the following symptoms/conditions: lung infection.The patient was prescribed Magnex (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Amikacin
.After starting to take Magnex the consumer reported adverse symptoms, such as: International Normalised Ratio IncreasedThese side effects may potentially be related to Magnex. The patient was hospitalized.
Magnex Side Effect Report#5524689-9
Septic Shock
This is a report of a 30-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: sepsis, who was treated with Magnex (dosage: NA, start time:
Oct 31, 2007), combined with:
  • Meronem
and developed a serious reaction and side effect(s): Septic Shock after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Magnex treatment in male patients, resulting in Death side effect.
Magnex Side Effect Report#5517616-1
Septic Shock
This report suggests a potential Magnex Septic Shock side effect(s) that can have serious consequences. A 30-year-old male patient (weight: NA) from India was diagnosed with the following symptoms/conditions: sepsis and used Magnex (dosage: NA) starting
Oct 31, 2007. After starting Magnex the patient began experiencing various side effects, including: Septic ShockAdditional drugs used concurrently:
  • Meronem
Although Magnex demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Septic Shock, may still occur.
Magnex Side Effect Report#5359577-4
Graft Haemorrhage, Haematuria
This Graft Haemorrhage problem was reported by a physician from India. A 80-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hydropneumothorax. On NS this consumer started treatment with Magnex (dosage: NA). The following drugs were being taken at the same time:
  • Enoxaparin Sodium (Daily Dose:.4ml)
  • Acetylsalicylic Acid/clopidogrel (Daily Dose:150mg)
  • I.v. Solutions
When using Magnex, the patient experienced the following unwanted symptoms/side effects: Graft Haemorrhage, HaematuriaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Graft Haemorrhage, may become evident only after a product is in use by the general population.
Magnex Side Effect Report#5223110-8
Disseminated Intravascular Coagulation, Haemorrhage Urinary Tract
This Disseminated Intravascular Coagulation side effect was reported by a physician from India. A 60-year-old male patient (weight:NA) experienced the following symptoms/conditions: respiratory tract infection.The patient was prescribed Magnex (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Amikacin
.After starting to take Magnex the consumer reported adverse symptoms, such as: Disseminated Intravascular Coagulation, Haemorrhage Urinary TractThese side effects may potentially be related to Magnex. The patient was hospitalized.
Magnex Side Effect Report#5223061-9
Haemorrhage, Platelet Count Decreased
This is a report of a 70-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: pneumonia aspiration, who was treated with Magnex (dosage: NA, start time: NS), combined with:
  • Amikacin
and developed a serious reaction and side effect(s): Haemorrhage, Platelet Count Decreased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Magnex treatment in male patients, resulting in Haemorrhage side effect. The patient was hospitalized.

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The appearance of Magnex 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.

    Magnex 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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    More About Magnex

    Side Effects reported to FDA: 49

    Magnex safety alerts: No

    Reported deaths: 14

    Reported hospitalizations: 7

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