Necrotising Fasciitis, Streptococcal Infection (6180982-0)
on Apr 24, 2009 Female patient from MALTA , 46 years of age, was diagnosed with

• epicondylitis

and was treated with Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone(View Usage). Patient experienced the following unwanted or unexpected effects: necrotising fasciitis, streptococcal infection (streptococcal infection Questions). Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone dosage: 2 Ml; Im.
Patient was taking other medications:

• AUGMENTIN '125' (View Augmentin '125' Review and Augmentin '125' Label )

Patient was hospitalized.

Eye Swelling, Feeling Hot, Lip Swelling, Swelling Face (5376664-5)
Patient was taking Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone (View Usage). Patient had the following side effects: eye swelling, feeling hot, lip swelling, swelling face on Jun 19, 2007 from PORTUGAL Additional patient health information: Female patient , 49 years of age, was diagnosed with

• pain (pain Questions)

and. Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone dosage: 1 Df; Im.
Patient was taking other medications:

• ALPRAZOLAM (CON.) (View Alprazolam (con.) Review and Alprazolam (con.) Label )
• WARFARIN (CON.) (View Warfarin (con.) Review and Warfarin (con.) Label )
• SERTRALINE HYDROCHLORIDE (CON.) (View Sertraline Hydrochloride (con.) Review and Sertraline Hydrochloride (con.) Label )
• AMBROXOL (CON.) (View Ambroxol (con.) Review and Ambroxol (con.) Label )
• AMOXICILLIN (CON.) (View Amoxicillin (con.) Review and Amoxicillin (con.) Label )

Patient was hospitalized.

Face Oedema (5309227-8)
Adverse event was reported on Apr 13, 2007 by a Female patient taking Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone (View Usage) (Dosage: 2 Ml;once;im) was diagnosed with

• myalgia

and. Location: PORTUGAL , 63 years of age, After Diprofos was administered, patient had the following side effects: face oedema.
Patient was taking other medications:

• CO DIOVAN (CON.) (View Co-diovan (con.) Review and Co-diovan (con.) Label )
• VIARTRIL (CON.) (View Viartril (con.) Review and Viartril (con.) Label )
• OMEPRAZOL (CON.) (View Omeprazol (con.) Review and Omeprazol (con.) Label )

Face Oedema (5271797-6)
on Mar 07, 2007 Female patient from PORTUGAL , 63 years of age, was diagnosed with

• myalgia

and was treated with Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone (View Usage). Patient experienced the following unwanted or unexpected effects: face oedema. Diprofos (betamethasone Sodium Phosphate/dipropionate) (betamethasone dosage: 2 Ml; Once; Im.
Patient was taking other medications:

• VALSARTAN AND HYDROCHLOROTHIAZIDE (View Valsartan And Hydrochlorothiazide Review and Valsartan And Hydrochlorothiazide Label )
• VIARTRIL (View Viartril Review and Viartril Label )
• OMEPRAZOLE (View Omeprazole Review and Omeprazole Label )

Diprofos Adverse Effect Reports (FDA)

Enter Unusual Symptoms or Side Effects:

Diprofos Information More About Diprofos Side Effects reported to FDA: 4. View FDA Adverse Reports Diprofos safety alerts: No Reported hospitalizations: 2 1 Dizziness 2 Diabetic 3 Diprophos 4 Swollen Face 5 IN BREATH 6 Change Of Taste 7 Diprofoss Injection Side Effect 8 Diprofos 9 Swollen Cheeks 10 Hiccup View More

Ask a Doctor 13 Doctors are Online Now. Current Wait time: 7 Minutes sever acne localized in the back heavy head especially on one side, then fatigue, rapid heart palpitations, sinus headache increase blood suga egzema View Diprofos Use Reports

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