Common Diprofos Side Effects

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

Face Oedema (2)
Streptococcal Infection (1)
Swelling Face (1)
Necrotising Fasciitis (1)
Lip Swelling (1)
Eye Swelling (1)
Feeling Hot (1)

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.

Diprofos Side Effects Reported to FDA

Diprofos Side Effect Report#6180982-0
Necrotising Fasciitis, Streptococcal Infection
This is a report of a 46-year-old patient (weight: NA) from Malta, suffering from the following health symptoms/conditions: epicondylitis, who was treated with Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone (dosage: 2 Ml; Im, start time: NS), combined with:
  • Augmentin '125'
and developed a serious reaction and side effect(s): Necrotising Fasciitis, Streptococcal Infection after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone treatment in patients, resulting in Necrotising Fasciitis side effect. The patient was hospitalized.
Diprofos Side Effect Report#5376664-5
Eye Swelling, Feeling Hot, Lip Swelling, Swelling Face
This report suggests a potential Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone Eye Swelling side effect(s) that can have serious consequences. A 49-year-old female patient (weight: NA) from Portugal was diagnosed with the following symptoms/conditions: pain and used Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone (dosage: 1 Df; Im) starting
Apr 09, 2007. After starting Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone the patient began experiencing various side effects, including: Eye Swelling, Feeling Hot, Lip Swelling, Swelling FaceAdditional drugs used concurrently:
  • Alprazolam (con.)
  • Warfarin (con.)
  • Sertraline Hydrochloride (con.)
  • Ambroxol (con.)
  • Amoxicillin (con.)
The patient was hospitalized. Although Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Eye Swelling, may still occur.
Diprofos Side Effect Report#5309227-8
Face Oedema
This Face Oedema problem was reported by a pharmacist from Portugal. A 63-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: myalgia. On
Jan 16, 2007 this consumer started treatment with Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone (dosage: 2 Ml;once;im). The following drugs were being taken at the same time:
  • Co-diovan (con.)
  • Viartril (con.)
  • Omeprazol (con.)
When using Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone, the patient experienced the following unwanted symptoms/side effects: Face OedemaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Face Oedema, may become evident only after a product is in use by the general population.
Diprofos Side Effect Report#5271797-6
Face Oedema
This Face Oedema side effect was reported by a pharmacist from Portugal. A 63-year-old female patient (weight:NA) experienced the following symptoms/conditions: myalgia.The patient was prescribed Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone (drug dosage: 2 Ml; Once; Im), which was initiated on
Jan 16, 2007. Concurrently used drugs:
  • Valsartan And Hydrochlorothiazide
  • Viartril
  • Omeprazole
.After starting to take Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone the consumer reported adverse symptoms, such as: Face OedemaThese side effects may potentially be related to Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone.

The appearance of Diprofos 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.

What are common Diprofos Side Effects for Women?

Women Side Effects Reports
Face Oedema 2
Eye Swelling 1
Feeling Hot 1
Lip Swelling 1
Swelling Face 1

What are common Diprofos Side Effects for Men?

Men Side Effects Reports

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.

    Diprofos 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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