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Solupred Side Effects

Common Solupred Side Effects


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

Abdominal Pain (3)
Diarrhoea (3)
Cough (3)
Alanine Aminotransferase Increased (2)
Aspartate Aminotransferase Increased (2)
Lipase Increased (2)
Purpura (2)
Rash Macular (2)
Pancreatitis Acute (2)
Intestinal Obstruction (1)
International Normalised Ratio Increased (1)
Penile Ulceration (1)
Ischaemic Stroke (1)
Infusion Related Reaction (1)
Pancreatitis (1)
Overdose (1)
Osteonecrosis (1)
Oedematous Pancreatitis (1)
Laceration (1)
Joint Tuberculosis (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.

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.

Solupred Side Effects Reported to FDA

The following Solupred 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.


The appearance of Solupred 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.
Overdose, Pneumonia, Hypoxia, Coma
This is a report of a 45-year-old male patient (weight: NA) from UNITED STATES, suffering from the following symptoms/conditions: pain, who was treated with Solupred /00016201/ (dosage: 60 Mg, Daily, start time: Dec 09, 2010), combined with:
  • Oxycontin (180 Mg, Q12h)
  • Oxycodone Hcl (60 Mg, Twice To Three Times Daily)
and developed a serious reaction and side effect(s). The consumer presented with:
  • Overdose
  • Pneumonia
  • Hypoxia
  • Coma
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Solupred /00016201/ treatment in male patients, resulting in overdose side effect. The patient was hospitalized.

Pancreatitis, Acute Respiratory Distress Syndrome
This report suggests a potential Solupred Pancreatitis, Acute Respiratory Distress Syndrome side effect(s) that can have serious consequences. A 81-year-old female patient (weight: NA) from FRANCE was diagnosed with the following symptoms/conditions: asthma and used Solupred (dosage: NA) starting NS. Soon after starting Solupred the patient began experiencing various side effects, including:
  • Pancreatitis
  • Acute Respiratory Distress Syndrome
Drugs used concurrently:
  • Diltiazem Hcl
  • Previscan
  • Lasilix
  • Elisor Tabs 20 Mg
  • Triatec
  • Pulmicort
  • Ventolin
The patient was hospitalized. Although Solupred demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as pancreatitis, may still occur.

Joint Tuberculosis
This Joint Tuberculosis problem was reported by a physician from UNITED KINGDOM. A 77-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: chronic lymphocytic leukaemia. On Nov 05, 2010 this consumer started treatment with Solupred (dosage: Unk). The following drugs were being taken at the same time:
  • Acetaminophen (Unk)
  • Effexor (Unk)
  • Lamaline (Unk)
  • Mabthera (Unk)
  • Cacit (Unk)
  • Nexium (Unk)
When commencing Solupred, the patient experienced the following unwanted symptoms/side effects:
  • Joint Tuberculosis
The 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 joint tuberculosis, may become evident only after a product is in use by the general population.

Pancreatitis Acute
This is a report of a 10-year-old male patient (weight: NA) from FRANCE. The patient developed the following symptoms/conditions: pyrexia,hypersensitivity and was treated with Solupred (dosage: NA) starting Feb 17, 2011. Concurrently used drugs:
  • Hydroxyzine
  • Cefpodoxime Proxetil
Soon after that, the consumer experienced the following side effects:
  • Pancreatitis Acute
The patient was hospitalized. This opens a possibility that Solupred treatment could cause the above reactions, including pancreatitis acute, and some male subjects may be more susceptible.


Intestinal Obstruction, Vomiting, Abdominal Rigidity, Oedematous Pancreatitis, Abdominal Pain, Faecaloma
A 81-year-old female patient (weight: NA) from FRANCE with the following symptoms/conditions: asthma,respiratory distress,hypercholesterolaemia started Solupred treatment (dosage: NA) on Mar 15, 2011. Soon after starting Solupred treatment, the subject experienced various side effects, including:
  • Intestinal Obstruction
  • Vomiting
  • Abdominal Rigidity
  • Oedematous Pancreatitis
  • Abdominal Pain
  • Faecaloma
Concurrently used drugs:
  • Terbutaline
  • Elisor
  • Diltiazem Hcl
  • Pulmicort
  • Budesonide
  • Ipratropium Bromide
  • Ventolin
  • Previscan
The patient was hospitalized. This finding indicates that some female patients could be more vulnerable to Solupred.

Anaemia, Gait Disturbance
A male patient from FRANCE (weight: NA) experienced symptoms, such as: renal transplant and was treated with Solupred(dosage: 5 Mg). The treatment was initiated on Dec 18, 2010. After that a consumer reported the following side effect(s):
  • Anaemia
  • Gait Disturbance
Concurrently used drugs, which potentially could have contributed to side effect(s) or affected Solupred efficacy:
  • Neoral (550 Mg, Unk)
  • Lasix
  • No Treatment Received
  • Cellcept (3 G, Daily)
The patient was hospitalized.

Proteinuria, Blood Creatinine Increased, Concomitant Disease Progression
In this report, Solupred was administered for the following condition: renal transplant.A male consumer from FRANCE (weight: NA) started Solupred treatment (dosage: 7.5 Mg, Daily) on Feb 09, 2011.Sometime after starting the treatment, the patient complained of the following side effect(s):
  • Proteinuria
  • Blood Creatinine Increased
  • Concomitant Disease Progression
A possible interaction with other drugs could have contributed to this reaction:
  • Cellcept (1.5 G, Daily)
  • Cellcept (5 G, Daily)
  • Cyclosporine (5 Mg, Daily)
  • Prograf (3 Mg, Bid)
The patient was hospitalized.Establishing a causal relationship between a specific drug and consumer's side effects is complex, but it is possible that in this report Solupred treatment could be related to the listed above side effect(s).

Diarrhoea, Cough, Rhinorrhoea, Pneumonitis, Pyrexia
This is a report of the following Solupred side effect(s):
  • Diarrhoea
  • Cough
  • Rhinorrhoea
  • Pneumonitis
  • Pyrexia
A male patient from FRANCE (weight: NA) presented with the following condition: NA and received a treatment with Solupred (dosage: NA) starting: Dec 02, 2010.The following concurrently used drugs could have generated interactions:
  • Cellcept (Unk)
  • Sandimmune (5 Mg Per Day)
  • Neoral (Unk)
The patient was hospitalized.This report suggests that a Solupred treatment could be associated with the listed above side effect(s).

Hypersensitivity, Dyspnoea, Cough, Abdominal Pain, Infusion Related Reaction, Tachycardia, Hypotension
This Solupred report was submitted by a 49-year-old male consumer from FRANCE (weight: NA). The patient was diagnosed with: NA and Solupred was administered (dosage: 15 Mg Per Day 3 Days Before Cycle) starting: NS. The consumer developed a set of symptoms:
  • Hypersensitivity
  • Dyspnoea
  • Cough
  • Abdominal Pain
  • Infusion Related Reaction
  • Tachycardia
  • Hypotension
Other drugs used simultaneously:
  • Infliximab, Recombinant (5 Mg/kg Depending On The Cycle)
  • Infliximab, Recombinant (5th Dose)
  • Infliximab, Recombinant
  • Hydrocortisone (100 Mg 30 Minutes Prior To Infliximab)
  • Atarax (30 Minutes Before Infliximab)
Those unexpected symptoms could be linked to a Solupred treatment, however establishing a potential drug-safety problem requires a more detailed clinical analysis.

Colitis Ischaemic, Diarrhoea
This is a report of a possible correlation between Solupred use and the following symptoms/side effect(s):
  • Colitis Ischaemic
  • Diarrhoea
which could contribute to an assessment of Solupred risk profile.A 80-year-old female consumer from FRANCE (weight: NA) was suffering from NA and was treated with Solupred (dosage: Unk Mg, Unk) starting Dec 29, 2010.Other concurrent medications:
  • Xarelto (1 Df, 1x/day)
  • Nexium (Unk)
  • Rocephin (Unk)
  • Actonel (Unk)
  • Neurontin (Unk)
  • Oxycontin (10 Mg, 2x/day)
  • Motilium (3 Df, 1x/day)
  • Eupressyl (Unk)


Abscess Intestinal, Ileal Perforation
A female patient from FRANCE (weight: NA) presented with the following symptoms: crohn's disease and after a treatment with Solupred (dosage: NA) experienced the following side effect(s):
  • Abscess Intestinal
  • Ileal Perforation
The treatment was started on Feb 01, 2010. Solupred was used in combination with the following drugs:
  • Humira
  • Pentasa
The patient was hospitalized.This report could alert potential Solupred consumers.

Haemothorax, Disease Progression
In this report, a 45-year-old male patient from FRANCE (weight: NA) was affected by a possible Solupred side effect.The patient was diagnosed with NA. After a treatment with Solupred (dosage: NA, start date: Jun 08, 2009), the patient experienced the following side effect(s):
  • Haemothorax
  • Disease Progression
The following simultaneously used drugs could have led to this reaction:
  • Docetaxel (Dose Unit: 75 Mg/m**2)
  • Actiskenan
  • Xanax
  • Forlax
  • Zophren
  • Fluticasone W/salmeterol
  • Bi Profenid
  • Speciafoldine
The patient was hospitalized.The findings here stress that side effects should be taken into consideration when evaluating a Solupred treatment.

Stevens-johnson Syndrome
This is a report of a 82-year-old male patient from FRANCE (weight: NA), who used Solupred (dosage: NA) for a treatment of bronchitis. After starting a treatment on Jan 19, 2010, the patient experienced the following side effect(s):
  • Stevens-johnson Syndrome
The following drugs could possibly have interacted with the Solupred treatment
  • Lasix
  • Rocephin
  • Domperidone
  • Allopurinol
  • Esomeprazole
  • Xatral
  • Lorazepam
  • Monicor
The patient was hospitalized.Taken together, these observations suggest that a Solupred treatment could be related to side effect(s), such as Stevens-johnson Syndrome.

Cytolytic Hepatitis, Pancreatitis Acute
This cytolytic hepatitis side effect was reported by a consumer or non-health professional from . A 53-year-old male patient (weight:NA) experienced the following symptoms/conditions: infection. The patient was prescribed Solupred /00016201/ (dosage: NA), which was started on Jan 18, 2009. Concurrently used drugs:
  • Telfast /01314201/
  • Amoxicilline Base
When starting to take Solupred /00016201/ the consumer reported the following symptoms:
  • Cytolytic Hepatitis
  • Pancreatitis Acute
The patient was hospitalized. These side effects may potentially be related to Solupred /00016201/.

Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Lipase Increased, Purpura, Rash Macular
This is a Solupred /00016201/ side effect report of a 64-year-old female patient (weight:NA) from , suffering from the following symptoms/conditions: NA, who was treated with Solupred /00016201/ (dosage:NA, start time: Aug 27, 2007), combined with:
  • Thiocolchicoside
  • Voltaren
  • Nexium
  • Telfast /01314201/
  • Pritorplus
  • Catapressan /00171101/
  • Atarax
  • Vastarel
, and developed a serious reaction and a alanine aminotransferase increased side effect. The patient presented with:
  • Alanine Aminotransferase Increased
  • Aspartate Aminotransferase Increased
  • Lipase Increased
  • Purpura
  • Rash Macular
which developed after the beginning of treatment. The patient was hospitalized. This side effect report can indicate a possible existence of increased vulnerability to Solupred /00016201/ treatment in female patients suffering from NA, resulting in alanine aminotransferase increased.

Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Lipase Increased, Purpura, Rash Macular
This report suggests a potential Solupred /00016201/ alanine aminotransferase increased side effect(s) that can have serious consequences. A 64-year-old female patient from (weight:NA) was diagnosed with the following health condition(s): NA and used Solupred /00016201/ (dosage: NA) starting Aug 27, 2007. Soon after starting Solupred /00016201/ the patient began experiencing various side effects, including:
  • Alanine Aminotransferase Increased
  • Aspartate Aminotransferase Increased
  • Lipase Increased
  • Purpura
  • Rash Macular
Drugs used concurrently:
  • Thiocolchicoside
  • Voltaren
  • Nexium
  • Telfast /01314201/
  • Pritorplus
  • Catapressan /00171101/
  • Atarax
  • Vastarel
The patient was hospitalized. Although Solupred /00016201/ demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as alanine aminotransferase increased, may still occur.

Abdominal Pain, Cough, Ecchymosis, Fall, Haematoma, Haemoglobin Decreased, International Normalised Ratio Increased, Laceration
This abdominal pain problem was reported by a consumer or non-health professional from . A 74-year-old female patient (weight: NA) was diagnosed with the following medical condition(s): bronchitis.On Feb 08, 2008 a consumer started treatment with Solupred /00016201/ (dosage: NA). The following drugs/medications were being taken at the same time:
  • Ketek
  • Previscan /00789001/
When commencing Solupred /00016201/, the patient experienced the following unwanted symptoms /side effects:
  • Abdominal Pain
  • Cough
  • Ecchymosis
  • Fall
  • Haematoma
  • Haemoglobin Decreased
  • International Normalised Ratio Increased
  • Laceration
The patient was hospitalized. Although all drugs are carefully tested before they are licensed for use, they carry potential side effect risks. Some side effects, such as abdominal pain, may become evident only after a product is in use by the general population.

Ischaemic Stroke, Speech Disorder
This is a Solupred /00016201/ side effect report of a 69-year-old male patient (weight: NA) from . The patient developed the following symptoms/conditions: NA and was treated with Solupred /00016201/ (dosage: NA) starting Feb 05, 2007. Concurrently used drugs:
  • Lovenox
  • Kardegic /00002703/
  • Carboplatine Dakota
  • Vastarel
  • Taxol
Soon after that, the consumer experienced the following of symptoms:
  • Ischaemic Stroke
  • Speech Disorder
The patient was hospitalized. This opens a possibility that Solupred /00016201/ could cause ischaemic stroke and that some male patients may be more susceptible.

Penile Ulceration, Rash Papular
A 63-year-old male patient (weight: NA) from FRANCE with the following symptoms: NA started Solupred treatment (dosage: 60 Mg, Daily (1/d)) on Jul 10, 2006. Soon after starting Solupred treatment, the consumer experienced several side effects, including:
  • Penile Ulceration
  • Rash Papular
. Concurrently used drugs:
  • Oxycontin (40 Mg, Daily (1/d))
  • Alimta (500 Mg/m2, Other)
  • Folic Acid
  • Vitamin B-12
  • Dexamethasone
This finding indicates that some patients can be more vulnerable to developing Solupred side effects, such as penile ulceration.

Agranulocytosis, Bone Marrow Disorder, Diarrhoea
This agranulocytosis side effect was reported by a consumer or non-health professional from . A 71-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Solupred (dosage: NA), which was started on Jul 28, 2006. Concurrently used drugs:
  • Imovane
  • Lantus
  • Xatral
  • Plavix
  • Detensiel
  • Amlor
  • Cellcept
  • Prograf
.When starting to take Solupred the consumer reported symptoms, such as:
  • Agranulocytosis
  • Bone Marrow Disorder
  • Diarrhoea
These side effects may potentially be related to Solupred. The patient was hospitalized.

Osteonecrosis, Wound Debridement
This is a report of a 74-year-old female patient (weight: NA) from , suffering from the following symptoms/conditions: multiple myeloma, who was treated with Solupred (dosage: NA, start time: Feb 20, 2004), combined with:
  • Antibiotics
  • Zometa (4 Mg, Qmo)
and developed a serious reaction and side effect(s). The consumer presented with:
  • Osteonecrosis
  • Wound Debridement
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Solupred treatment in female patients, resulting in osteonecrosis side effect. The patient was hospitalized.



Keep Track of Side Effects

Note Your Observations

It is really important to keep of your 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

    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.


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