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Diprofos Side Effects

Report Diprofos Side Effects

If you experienced any harmful or unwanted effects of Diprofos, please share your experience. This could help to raise awareness about Diprofos side effects, identify uknown risks and inform health professionals and patients taking Diprofos.

Examples: headache, dizziness


The most commonly reported Diprofos side effects are:
Diabetic (41 reports)
Swollen Face (24 reports)
Diprophos (23 reports)
Dizziness (19 reports)
Change Of Taste (14 reports)
Insomnia (14 reports)
IN BREATH (12 reports)
Hiccup (5 reports)
Sever Pain In All My Body Mucles (5 reports)

If you have experienced a side effect listed above, you can check a box to report it.


To view a complete list of submitted side effects, please follow the link Diprofos side effects . You can also compare Diprofos side effects or view FDA reports.

Diprofos Side Effects reported to FDA

The following Diprofos reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
The 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 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 identified a causal relationship between the drug and the listed risk.

Necrotising Fasciitis, Streptococcal Infection
on Apr 24, 2009 Patient from MALTA , 46 years of age, was diagnosed with and was treated with Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone. Directly after, patient experienced the unwanted or unexpected Diprofos side effects: necrotising fasciitis, streptococcal infection. Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone dosage: 2 Ml; Im.
Associated medications used: Patient was hospitalized.

Eye Swelling, Feeling Hot, Lip Swelling, Swelling Face
Patient was taking Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone. Patient felt the following Diprofos side effects: eye swelling, feeling hot, lip swelling, swelling face on Jun 19, 2007 from PORTUGAL Additional patient health information: Female , 49 years of age, was diagnosed with and. Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone dosage: 1 Df; Im.
Multiple prescriptions taken:
  • Alprazolam (con.)
  • Warfarin (con.)
  • Sertraline Hydrochloride (con.)
  • Ambroxol (con.)
  • Amoxicillin (con.)
Patient was hospitalized.

Face Oedema
Adverse event was reported on Apr 13, 2007 by a Female taking Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone (Dosage: 2 Ml;once;im) was diagnosed with and. Location: PORTUGAL , 63 years of age, After Diprofos was administered, patient encountered several Diprofos side effects: face oedema.
Multiple concurrent drugs taken:

Face Oedema
on Mar 07, 2007 Female from PORTUGAL , 63 years of age, was diagnosed with and was treated with Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone. Directly after, patient experienced the unwanted or unexpected Diprofos side effects: face oedema. Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone dosage: 2 Ml; Once; Im.
Associated medications used:

Record and Track Your Side Effects

It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.

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Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.

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.

Tips for Taking Medicines Properly

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