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Fluorescein adverse events reported to FDA.

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Summary

FDA Adverse Reports: 13. View All

Fluorescein FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 6

More About Fluorescein

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1I Had A Very Allergic Reaction To Fluorescein. I Was Given A Shot Of Benadryl In The Doctor's Office, But I Coutinued To Itch And Swell. They Took Me To The ER Where I Was Observed And Given Prednisone.
2Double Vision
3SHINGLES
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Often additional risks of using a medication, such as Fluorescein, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Fluorescein users, Learn more about unwanted side effects & find ways to reduce them. Browse Fluorescein Adverse Reports reported to FDA and participate in Fluorescein discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Fluorescein. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Fluorescein Adverse Effect Reports (FDA)

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6444619-5 | Chest Discomfort, Dry Mouth, Hypersensitivity, Pruritus, Urticaria
on Nov 17, 2009 Male patient from UNITED STATES , 83 years of age, was diagnosed with angiogram and was treated with Fluorescein (View Usage). Patient experienced the following unwanted or unexpected effects: chest discomfort, dry mouth, hypersensitivity, pruritus, urticaria. Fluorescein dosage: .

6390498-4 | Anaphylactic Reaction, Cardio-respiratory Arrest, Cough, Hyperhidrosis, Hypotension, Immediate Post-injection Reaction, Renal Failure Acute, Retching
Patient was taking Fluorescein (View Usage). Patient had the following side effects: anaphylactic reaction, cardio-respiratory arrest, cough, hyperhidrosis, hypotension, immediate post-injection reaction, renal failure acute, retching on Oct 05, 2009 from UNITED STATES Additional patient health information: Male patient , 62 years of age, was diagnosed with angiogram and. Fluorescein dosage: 5 Once Iv. Patient was hospitalized.

6229227-3 | Dizziness, Dyspnoea, Lethargy, Syncope
Adverse event was reported on Jun 11, 2009 by a Male patient taking Fluorescein (View Usage) (Dosage: ) . Location: UNITED STATES , 88 years of age, weighting 241.3 lb, After Fluorescein was administered, patient had the following side effects: dizziness (What is dizziness?), dyspnoea, lethargy, syncope. Patient was hospitalized.

6182393-0 | Anaphylactic Reaction, Angioedema, Burning Sensation, Cardio-respiratory Arrest, Confusional State, Consciousness Fluctuating, Dyspnoea, Hyperhidrosis, Infusion Related Reaction
on May 05, 2009 Male patient from UNITED STATES , 81 years of age, weighting 172.0 lb, was diagnosed with imaging procedure, ophthalmological examination and was treated with Fluorescein (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic reaction, angioedema, burning sensation, cardio-respiratory arrest, confusional state, consciousness fluctuating, dyspnoea, hyperhidrosis, infusion related reaction. Fluorescein dosage: Once Iv. Patient was hospitalized.


5724616-5 | Blood Pressure Decreased, Cold Sweat, Diarrhoea, Heart Rate Decreased, Hyperglycaemia, Nausea, Oxygen Saturation Decreased, Pruritus
on Apr 30, 2008 Female patient from UNITED STATES , 75 years of age, was diagnosed with angiogram and was treated with Fluorescein (View Usage). Patient had the following side effects: blood pressure decreased, cold sweat, diarrhoea, heart rate decreased, hyperglycaemia, nausea (What is nausea?), oxygen saturation decreased, pruritus. Fluorescein dosage: 500 Mg Ivp X1. During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), MEVACOR (View Mevacor Review and Mevacor Label ), DIOVAN (View Diovan Review and Diovan Label ), LANTUS (View Lantus Review and Lantus Label ), NOVOLOG (View Novolog Review and Novolog Label ).

5485610-5 | Chills, Cold Sweat, Confusional State, Dry Mouth, Fatigue, Feeling Abnormal, Feeling Cold, Headache, Hyperhidrosis
Patient was taking Fluorescein (View Usage). After Fluorescein was administered, patient had the following side effects: chills, cold sweat, confusional state, dry mouth, fatigue, feeling abnormal, feeling cold, headache (What is headache?), hyperhidrosis on Oct 11, 2007 from UNITED STATES Additional patient health information: Female patient , 23 years of age, weighting 135.0 lb, was diagnosed with ophthalmological examination and. Fluorescein dosage: Eye Drop Once Ophthalmic. During the same period patient was treated with PROPARACAINE HCL (Eye Drop Once Ophthalmic) (View Proparacaine Hcl Review and Proparacaine Hcl Label ).

5139844-X | Asthenia, Blood Pressure Increased, Chromaturia, Dehydration, Dizziness, Loss Of Consciousness, Oral Intake Reduced, Pallor, Periorbital Oedema
Adverse event was reported on Oct 25, 2006 by a Male patient taking Fluorescein (View Usage) (Dosage: 500 Mg Ivp Over 5-7 Sec X 1 Dose At 3:35 Pm) was diagnosed with angiogram and. Location: UNITED STATES , 83 years of age, weighting 153.2 lb, Patient experienced the following unwanted or unexpected effects: asthenia, blood pressure increased, chromaturia, dehydration, dizziness (What is dizziness?), loss of consciousness, oral intake reduced, pallor, periorbital oedema. During the same period patient was treated with LOSARTAN POSTASSIUM (View Losartan Postassium Review and Losartan Postassium Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), OCUVITE (View Ocuvite Review and Ocuvite Label ), BUPROPION HCL (View Bupropion Hcl Review and Bupropion Hcl Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ).

5135686-X | Blood Pressure Diastolic Increased, Cough, Erythema, Somnolence, Throat Irritation, Throat Tightness, Urticaria
on Oct 24, 2006 Female patient from UNITED STATES , 50 years of age, was diagnosed with angiogram and was treated with Fluorescein (View Usage). Patient had the following side effects: blood pressure diastolic increased, cough, erythema, somnolence, throat irritation, throat tightness, urticaria. Fluorescein dosage: 5 Ml Iv. During the same period patient was treated with ERGOCALCIFEROL (View Ergocalciferol Review and Ergocalciferol Label ), CALCIUM (View Calcium Review and Calcium Label ), LORATADINE (View Loratadine Review and Loratadine Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ).

4951894-2 | Asthenia, Blood Pressure Decreased, Dizziness, Pallor
on Mar 22, 2006 Female patient from UNITED STATES , 15 years of age, weighting 103.6 lb, was diagnosed with angiogram retina and was treated with Fluorescein (View Usage). After Fluorescein was administered, patient had the following side effects: asthenia, blood pressure decreased, dizziness (What is dizziness?), pallor. Fluorescein dosage: 3 Ml Ivp X1 Dose. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), IBUPROFEN PRN (View Ibuprofen Prn Review and Ibuprofen Prn Label ), MULTIVITAMIN PRN (View Multivitamin Prn Review and Multivitamin Prn Label ).

4915072-5 | Asthenia
Patient was taking Fluorescein (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia on Feb 15, 2006 from UNITED STATES Additional patient health information: Female patient , weighting 186.0 lb, was diagnosed with eye operation and. Fluorescein dosage: Iv X1 Dose. Patient was hospitalized.

4832362-5 | Blood Pressure Increased, Cardio-respiratory Arrest, Convulsion, Headache, Heart Rate Increased, Loss Of Consciousness, Moaning
Adverse event was reported on Nov 16, 2005 by a Male patient taking Fluorescein (View Usage) (Dosage: ) was diagnosed with angiogram and. Location: UNITED STATES , 56 years of age, Patient had the following side effects: blood pressure increased, cardio-respiratory arrest, convulsion, headache (What is headache?), heart rate increased, loss of consciousness, moaning. During the same period patient was treated with NS (View Ns Review and Ns Label ).

4731441-0 | Respiratory Arrest
on Aug 01, 2005 Male patient from UNITED STATES , 65 years of age, weighting 220.0 lb, was treated with Fluorescein (View Usage). After Fluorescein was administered, patient had the following side effects: respiratory arrest. Fluorescein dosage: .

4667297-4 | Cardio-respiratory Arrest, Infusion Related Reaction, Urticaria
on May 19, 2005 Male patient from , 70 years of age, was diagnosed with angiogram and was treated with Fluorescein (View Usage). Patient experienced the following unwanted or unexpected effects: cardio-respiratory arrest, infusion related reaction, urticaria. Fluorescein dosage: Iv Once. Patient was hospitalized.


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Fluorescein Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

Annonymous   Las Vegas, Nevada 

2:41pm on Thursday, May 14th, 2009

When the Optometrist has inserted the eye drops I felt weird to start with. When she put the contact... read more »

To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Fluorescein risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Fluorescein quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Fluorescein use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Fluorescein Reactions
Anaphylactic Reaction
Angioedema
Asthenia
Blood Pressure Decreased
Blood Pressure Diastolic Increased
Blood Pressure Increased
Burning Sensation
Cardio-respiratory Arrest
Chest Discomfort
Chills
Chromaturia
Cold Sweat
Confusional State
Consciousness Fluctuating
Convulsion
Cough
Dehydration
Diarrhoea
DizzinessWhat is Dizziness?
Dry Mouth
Dyspnoea
Erythema
Fatigue
HeadacheWhat is Headache?
Hyperhidrosis
Infusion Related Reaction
Loss Of Consciousness
Pallor
Pruritus
Urticaria
Fluorescein Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Fluorescein adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!