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From FDA reports: side effects of Urimax-f Cipla for a Male patient aged 50

This is a personalized study for a 50 year old male patient. The study is created by eHealthMe based on reports of 12,686 people who take the same drug and have side effectsfrom FDA.

On Oct, 13, 2014: 12,686 people who reported to have side effects when taking Urimax-f Cipla are studied

Trend of Urimax-f Cipla's drug interactions, side effects, and effectiveness reports (3987436)

Information of the patient in this study:

Age: 50

Gender: male

Conditions: Benign Prostatic Hyperplasia

Drugs taking:
- Urimax-f Cipla: used for < 1 month

Side effects have: Semen Volume Decreased, Erectile Dysfunction

eHealthMe real world results:

Comparison with this patient's adverse outcomes among males aged 50 (±5):

Side effectNumber of reports
Semen Volume Decreased2 (0.11%)
Erectile Dysfunction8 (0.46%)

Most common side effects experienced by males aged 50 (±5) in the use of Urimax-f Cipla:

Side effectNumber of reports
Pyrexia (fever)360
Myocardial Infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)170
Nausea (feeling of having an urge to vomit)148
Aspartate Aminotransferase Increased144
Lipodystrophy Acquired (a regional loss of subcutaneous adipose tissue which usually starts in the face, extends downward acquired)142
Malaise (a feeling of general discomfort or uneasiness)140
Fatigue (feeling of tiredness)137
Immune Reconstitution Syndrome (immune recovery syndrome)134
Alanine Aminotransferase Increased130
Condition Aggravated (worse condition)124

Most common side effects experienced by males aged 50 (±5) in long term use of Urimax-f Cipla:

Side effectNumber of reports
Myocardial Infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)38
Diarrhoea24
Abnormal Dreams20
Anaemia (lack of blood)18
Renal Failure Acute (rapid kidney dysfunction)14
Gamma-glutamyltransferase Increased14
General Physical Health Deterioration (weak health status)12
Hypokalaemia (low potassium)12
Vomiting11
Neutropenia (an abnormally low number of neutrophils)10

For people in general (regardless of gender or age):

Comparison with this patient's adverse outcomes:

Side effectNumber of reports
Semen Volume Decreased2 (0.02%)
Erectile Dysfunction32 (0.25%)

Most common side effects experienced by people in the use of Urimax-f Cipla:

Side effectNumber of reports
Pyrexia (fever)2,359
Nausea (feeling of having an urge to vomit)1,304
Pregnancy1,198
Vomiting1,139
Vomiting Nos1,129
Diarrhoea1,033
Immune Reconstitution Syndrome (immune recovery syndrome)924
Asthenia (weakness)913
Lactic Acidosis (low ph in body tissues)838
Drug Exposure During Pregnancy832

Most common side effects experienced by people in long term use of Urimax-f Cipla:

Side effectNumber of reports
Pyrexia (fever)150
Pregnancy150
Abortion Spontaneous (naturally occurring miscarriage)132
Drug Exposure During Pregnancy118
Abortion Induced (medically referred abortion)114
Lactic Acidosis (low ph in body tissues)102
Diarrhoea84
Nausea (feeling of having an urge to vomit)78
Nervous System Disorder (a general class of medical conditions affecting the nervous system)78
Gamma-glutamyltransferase Increased76

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

You can also:

NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also considered.

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

 

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