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Cefprozil

Popular Brands: : Cefzil, Cefprozil, Procef, Brisoral
Official FDA Reports3,433
Social Media Events221
Total Posts145
Avg. Review Score2.16/ 5

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Cefzil.

* Extracted from FDA Adverse Event Report

Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (FAERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


The proportion of people completing user reviews who complained about a side effect.

The proportion of social media adverse event complaints for each adverse event type.

The proportion of FAERS (FDA) adverse event complaints for each adverse event type.


Cefprozil Side Effects

  Social Media
(Online Comments)
FAERS
(Reports Submitted to FDA)
Side Effect On Drug
Label
Overall
Alarm
Reports % of
Reports
Alarm Reports % of
Reports
Alarm

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


User Voices

The following are comments from users that experienced side effects while taking Cefprozil

Nausea

Side Effects: Made me feel a little nauseas on an empty stomach.

It got rid of a terrible ear infection. After 3 days, my ear infection pain was greatly diminished, but I kept taking ...


Source: Cefzil (Cefprozil)

View full report on Cefprozil related nausea

Did the author experience nausea while taking cefprozil?

What is this?

Headache

Side Effects: Horrible nausea on the 3rd day until the last day of taking the medication. Tired all the time, and severe headache .


Source: CEFZIL: Side effects, ratings, and pat...

View full report on Cefprozil related headache

Did the author experience headache while taking cefzil?

What is this?

Somnolence

Side Effects: Horrible nausea on the 3rd day until the last day of taking the medication. Tired all the time, and severe headache.


Source: CEFZIL: Side effects, ratings, and pat...

View full report on Cefprozil related somnolence

Did the author experience somnolence while taking cefzil?

What is this?

Tell us about your Experience with Cefprozil

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Headache, Nausea, Somnolence

Posted By Anonymous in askapatient.com on April 9, 2015 @ 12:00 am

Side Effects: Horrible nausea on the 3rd day until the last day of taking the medication. Tired all the time, and severe headache.

Druginformer Identified Side Effects: Vomiting, Fatigue

Posted By Anonymous in askapatient.com on March 19, 2015 @ 12:00 am

Side Effects: Day three on antibiotic, haven't noticed anything other than extreme fatigue which could be from being sick. Hoping it goes well..

Druginformer Identified Side Effects: Hypersensitivity, Urticaria, Hypertension, Rash

Posted By Anonymous in askapatient.com on January 28, 2015 @ 12:00 am

... rash on calves and thighs. Took Benadryl. Next morning, it had spread to hands, arms, under arms, stomach, etc. Returned to dr. Blood pressure was high (152/102). He added the allergy to my file. R...

Druginformer Identified Side Effects: Headache, Nausea, Somnolence

Posted By Anonymous in askapatient.com on December 21, 2014 @ 12:00 am

Side Effects: Extreme tiredness ,nausea and headache . The infection seems to have gone but the side effects are horrible !

Druginformer Identified Side Effects: Feeling cold, Somnolence

Posted By Anonymous in askapatient.com on December 13, 2014 @ 12:00 am

... Within 15-20 minutes of taking Cefprozil I was uncontrollably sleepy and went to bed. I woke at around 6 am and took my next 12 hour dose. Within 30 minutes I was out cold asleep again. I'm glad it is...

Druginformer Identified Side Effects: Urticaria

Posted By Anonymous in askapatient.com on October 22, 2014 @ 12:00 am

Severe hives after day 7 on the med.hives from head to toes eyes lips with difficulty to swallow. Almost end up at ER. my doctor gave me total of 3 shots of adrenalin within 48 hours t...

Druginformer Identified Side Effects: Pain, Sleep disorder, Gastroenteritis, Diarrhoea, Discomfort

Posted By Anonymous in askapatient.com on October 17, 2014 @ 12:00 am

Side Effects: I took cefzil on two occasions, the first one sent me to the ER uncontrollable vomiting; I have never been in that much pain and they gave me Benadryl by IV and Rocephen and said I had ...

Druginformer Identified Side Effects: Pruritus, Urticaria, Swelling

Posted By Anonymous in askapatient.com on June 7, 2014 @ 12:00 am

Side Effects: Full body of itchy hives + swelling of the lips

Druginformer Identified Side Effects: Hypersensitivity, Somnolence

Posted By Anonymous in askapatient.com on May 7, 2014 @ 12:00 am

... my eyes open. Its harder to wake up in the morning too, since I started this. Only day 5 today, hope my symptoms don't get worse like most of you are saying!!! Plus I am allergic to penicillin and I k...

Druginformer Identified Side Effects: Vomiting, Rash, Urine output

Posted By Anonymous in askapatient.com on December 19, 2013 @ 12:00 am

... then after his first dose on the 9th day that evening he started to vomit and while he was vomiting he would have a red hivey rash that would disappear after he finished throwing up, I have noticed he...


Additional Drug Information


* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.