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From FDA reports: drug interactions between Ativan, Potassium Chloride, Pliva Prescription Strength Vitamin D Barr Pharmaceuticals New Jersey for a Female patient aged 45

This is a personalized study for a 45 year old female patient. The study is created by eHealthMe based on reports of 587 people who take the same drugs and have drug interactionsfrom FDA.

On Aug, 11, 2014: 587 people who reported to have interactions when taking Ativan, Potassium Chloride, Pliva Prescription Strength Vitamin D Barr Pharmaceuticals New Jersey are studied

Trend of Ativan, Potassium Chloride, Pliva Prescription Strength Vitamin D Barr Pharmaceuticals New Jersey's drug interactions, side effects, and effectiveness reports (3051943)

Information of the patient in this study:

Age: 45

Gender: female

Drugs taking:
- Ativan
- Potassium Chloride
- Pliva Prescription Strength Vitamin D Barr Pharmaceuticals New Jersey

Drug interactions have: Visual Impairment, Lymphadenopathy, Blood Arsenic Increased

eHealthMe real world results:

Comparison with this patient's adverse outcomes among females aged 45 (±5):

InteractionNumber of reports
Visual Impairment4 (11.43%)
Lymphadenopathy (disease or enlargement of lymph nodes)3 (8.57%)
Blood Arsenic Increased2 (5.71%)

Most common interactions experienced by females aged 45 (±5) in the use of Ativan, Potassium Chloride, Pliva Prescription Strength Vitamin D Barr Pharmaceuticals New Jersey:

InteractionNumber of reports
Diarrhoea24
Dyspnoea (difficult or laboured respiration)24
Vomiting18
Nausea (feeling of having an urge to vomit)18
Pneumonia15
Abdominal Pain12
Loss Of Consciousness10
Pain10
Insomnia (sleeplessness)10
Vision Blurred8

Most common interactions experienced by females aged 45 (±5) in long term use of Ativan, Potassium Chloride, Pliva Prescription Strength Vitamin D Barr Pharmaceuticals New Jersey:

None.

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

Comparison with this patient's adverse outcomes:

InteractionNumber of reports
Visual Impairment64 (10.90%)
Lymphadenopathy (disease or enlargement of lymph nodes)51 (8.69%)
Blood Arsenic Increased2 (0.34%)

Most common interactions experienced by people in the use of Ativan, Potassium Chloride, Pliva Prescription Strength Vitamin D Barr Pharmaceuticals New Jersey:

InteractionNumber of reports
Dyspnoea (difficult or laboured respiration)378
Asthenia (weakness)343
Vomiting315
Anxiety302
Pain278
Nausea (feeling of having an urge to vomit)262
Fatigue (feeling of tiredness)258
Diarrhoea255
Anaemia (lack of blood)210
Pneumonia195

Most common interactions experienced by people in long term use of Ativan, Potassium Chloride, Pliva Prescription Strength Vitamin D Barr Pharmaceuticals New Jersey:

InteractionNumber of reports
Dyspnoea (difficult or laboured respiration)4
Anxiety4
Fatigue (feeling of tiredness)4
Orthostatic Hypotension (a medical condition consisting of a sudden decrease in blood pressure when a person stands up)4
Non-small Cell Lung Cancer (type of epithelial lung cancer)3
Respiratory Failure (inadequate gas exchange by the respiratory system)3
Disease Progression2

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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