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Sarafem adverse events reported to FDA.

Have You Experienced unusual Sarafem symptoms? PatientsVille.com collects and analyzes Sarafem side effect and adverse reports submitted by Sarafem users, such as .

Summary

FDA Adverse Reports: 17. View All

Sarafem FDA safety alerts: No

Reported deaths: 4

Reported hospitalizations: 6

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Often additional risks of using a medication, such as Sarafem, 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 Sarafem users, Learn more about unwanted side effects & find ways to reduce them. Browse Sarafem Adverse Reports reported to FDA and participate in Sarafem discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Sarafem. 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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Sarafem Adverse Effect Reports (FDA)

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6474763-8 | Arrhythmia, Bradycardia, Bronchopneumonia, Cardio-respiratory Arrest, Cardiomegaly, Diarrhoea, Hypotension, Hypoxia
on May 05, 2009 Female patient from UNITED STATES , weighting 11.07 lb, was treated with Sarafem (View Usage). Patient experienced the following unwanted or unexpected effects: arrhythmia (What is arrhythmia?), bradycardia, bronchopneumonia, cardio-respiratory arrest, cardiomegaly, diarrhoea, hypotension, hypoxia. Sarafem dosage: . Patient was hospitalized.

6460542-4 | Cardiac Arrest, Hypoxic Encephalopathy, Truncus Arteriosus Persistent, Ventricular Septal Defect
Patient was taking Sarafem (View Usage). Patient had the following side effects: cardiac arrest (What is cardiac arrest?), hypoxic encephalopathy, truncus arteriosus persistent, ventricular septal defect on Nov 25, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 11.00 lb, was diagnosed with postpartum depression (What is postpartum depression?) and. Sarafem dosage: 20 Mg Once A Day Po. Patient was hospitalized and became disabled.

6409677-2 | Asthenia, Depression, Serotonin Syndrome, Treatment Noncompliance
Adverse event was reported on Oct 21, 2009 by a Female patient taking Sarafem (View Usage) (Dosage: 20mg Qd Po) was diagnosed with premenstrual syndrome (What is premenstrual syndrome?), migraine without aura and. Location: UNITED STATES , weighting 128.0 lb, After Sarafem was administered, patient had the following side effects: asthenia, depression (What is depression?), serotonin syndrome, treatment noncompliance. During the same period patient was treated with MAXALT (10mg Qd- Tid Prn Po) (View Maxalt Review and Maxalt Label ). Patient was hospitalized.

6353988-6 | Bradycardia, Cardio-respiratory Arrest, Cardiomegaly, Choking, Cyanosis, Dyspnoea, Hypotension, Right Aortic Arch
on Sep 01, 2009 Female patient from UNITED STATES , weighting 7.56 lb, was treated with Sarafem (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, cardio-respiratory arrest, cardiomegaly, choking (What is choking?), cyanosis, dyspnoea, hypotension, right aortic arch. Sarafem dosage: 20 Mg, Daily (1/d). During the same period patient was treated with PRENATAL VITAMINS /01549301/ (View Prenatal Vitamins /01549301/ Review and Prenatal Vitamins /01549301/ Label ), PROGESTERONE (View Progesterone Review and Progesterone Label ). Patient was hospitalized.


6191880-0 | Arrhythmia, Bradycardia, Bronchopneumonia, Cardio-respiratory Arrest, Cardiomegaly, Diarrhoea, Hypotension, Hypoxia
on May 05, 2009 Female patient from UNITED STATES , weighting 11.07 lb, was treated with Sarafem (View Usage). Patient had the following side effects: arrhythmia (What is arrhythmia?), bradycardia, bronchopneumonia, cardio-respiratory arrest, cardiomegaly, diarrhoea, hypotension, hypoxia. Sarafem dosage: . Patient was hospitalized.

6073022-5 | Depression, Diarrhoea, Hyperhidrosis, Movement Disorder, Palpitations, Panic Attack, Serotonin Syndrome, Tachyphrenia
Patient was taking Sarafem (View Usage). After Sarafem was administered, patient had the following side effects: depression (What is depression?), diarrhoea, hyperhidrosis, movement disorder (What is movement disorder?), palpitations, panic attack, serotonin syndrome, tachyphrenia on Feb 09, 2009 from UNITED STATES Additional patient health information: Female patient , 37 years of age, weighting 130.0 lb, was diagnosed with premenstrual syndrome (What is premenstrual syndrome?), migraine (What is migraine?) and. Sarafem dosage: 7 Day Or 14 Day Before Period One A Day Po. During the same period patient was treated with ZOMIG (Prn For Migraines Onset Po) (View Zomig Review and Zomig Label ).

5911666-9 | Corneal Abrasion, Dry Eye, Eye Irritation, Eye Pain, Keratorhexis, No Therapeutic Response, Somnolence, Vision Blurred
Adverse event was reported on Sep 18, 2008 by a Female patient taking Sarafem (View Usage) (Dosage: 10 Mg Qd, Oral) was diagnosed with premenstrual syndrome (What is premenstrual syndrome?) and. Location: UNITED STATES , 52 years of age, Patient experienced the following unwanted or unexpected effects: corneal abrasion, dry eye, eye irritation, eye pain, keratorhexis, no therapeutic response, somnolence, vision blurred. During the same period patient was treated with SAREFEM /00724401/ (FLUOXETINE) CAPSULE, 10MG (View Sarefem /00724401/ (fluoxetine) Capsule, 10mg Review and Sarefem /00724401/ (fluoxetine) Capsule, 10mg Label ).

5898216-0 | Dysgeusia, Pharyngeal Oedema, Throat Irritation
on Jul 15, 2008 Female patient from UNITED STATES , 47 years of age, was treated with Sarafem (View Usage). Patient had the following side effects: dysgeusia, pharyngeal oedema, throat irritation. Sarafem dosage: 2 Tablets, Qd, Oral.

5771266-0 | Dysgeusia, Foreign Body Trauma, Pharyngeal Oedema, Throat Irritation
on Jun 12, 2008 Female patient from UNITED STATES , 47 years of age, was treated with Sarafem (View Usage). After Sarafem was administered, patient had the following side effects: dysgeusia, foreign body trauma, pharyngeal oedema, throat irritation. Sarafem dosage: Two Tablets By Mouth Daily.

5699150-1 | Dizziness, Dyspnoea, Heart Rate Increased, Thirst
Patient was taking Sarafem (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), dyspnoea, heart rate increased, thirst on Apr 07, 2008 from UNITED STATES Additional patient health information: Female patient , 47 years of age, weighting 135.0 lb, was diagnosed with listless and. Sarafem dosage: One Pill Daily Po.

5347621-X | Anorexia, Feeling Abnormal, Insomnia, Irritability, Suicidal Ideation, Weight Decreased
Adverse event was reported on Jun 04, 2007 by a Female patient taking Sarafem (View Usage) (Dosage: ) was diagnosed with prophylaxis, stress (What is stress?) and. Location: UNITED STATES , 25 years of age, weighting 110.0 lb, Patient had the following side effects: anorexia, feeling abnormal, insomnia, irritability, suicidal ideation, weight decreased.

5078592-1 | Apathy, Blepharospasm, Dyskinesia, Eyelid Function Disorder, Facial Pain, Feeling Abnormal, Hallucination, Visual, Headache
on Aug 09, 2006 Female patient from UNITED STATES , 46 years of age, weighting 130.0 lb, was diagnosed with premenstrual syndrome (What is premenstrual syndrome?), attention deficit/hyperactivity disorder and was treated with Sarafem (View Usage). After Sarafem was administered, patient had the following side effects: apathy, blepharospasm, dyskinesia, eyelid function disorder, facial pain, feeling abnormal, hallucination, visual, headache (What is headache?). Sarafem dosage: 10 Mg 1x Daily Po. During the same period patient was treated with CONCERTA (18 Mg 2 X Daily Po) (View Concerta Review and Concerta Label ), MAXALT MLT (View Maxalt-mlt Review and Maxalt-mlt Label ), NAPROXEN (View Naproxen Review and Naproxen Label ), RENOVA (View Renova Review and Renova Label ), EXCEDRINE EXTRA STRENGTH (View Excedrine Extra Strength Review and Excedrine Extra Strength Label ).

4784963-0 | Caesarean Section, Foetal Heart Rate Deceleration
on Sep 14, 2005 Female patient from UNITED STATES , weighting 4.41 lb, was treated with Sarafem (View Usage). Patient experienced the following unwanted or unexpected effects: caesarean section, foetal heart rate deceleration. Sarafem dosage: Unk. During the same period patient was treated with PRENATAL VITAMINS (View Prenatal Vitamins Review and Prenatal Vitamins Label ), ZOFRAN (View Zofran Review and Zofran Label ).

4753382-5 | Deafness, Menstrual Disorder, Migraine, Nerve Injury, Off Label Use, Vocal Cord Thickening
Patient was taking Sarafem (View Usage). Patient had the following side effects: deafness, menstrual disorder, migraine (What is migraine?), nerve injury, off label use, vocal cord thickening on Aug 08, 2005 from UNITED STATES Additional patient health information: Female patient , 17 years of age, was diagnosed with mood swings and. Sarafem dosage: 40 Mg. During the same period patient was treated with ADDERALL 10 (View Adderall 10 Review and Adderall 10 Label ), SINGULAIR (View Singulair Review and Singulair Label ), PULMOCORTISON INY (View Pulmocortison Iny Review and Pulmocortison Iny Label ), PREVACID (View Prevacid Review and Prevacid Label ), ALLEGRA (View Allegra Review and Allegra Label ).

4665696-8 | Crying, Feeling Abnormal, Gastric Bypass, Weight Increased
Adverse event was reported on May 03, 2005 by a Female patient taking Sarafem (View Usage) (Dosage: ) was diagnosed with premenstrual syndrome (What is premenstrual syndrome?) and. Location: , 39 years of age, After Sarafem was administered, patient had the following side effects: crying, feeling abnormal, gastric bypass, weight increased. During the same period patient was treated with PROZAC (View Prozac Review and Prozac Label ). Patient was hospitalized.

4648979-7 | Caesarean Section, Foetal Heart Rate Decreased, Small For Dates Baby
on Apr 13, 2005 Female patient from , weighting 4.41 lb, was treated with Sarafem (View Usage). Patient experienced the following unwanted or unexpected effects: caesarean section, foetal heart rate decreased, small for dates baby. Sarafem dosage: . During the same period patient was treated with PRENATAL VITAMINS (View Prenatal Vitamins Review and Prenatal Vitamins Label ), ZOFRAN (View Zofran Review and Zofran Label ).

4579437-6 | Cerebrovascular Accident, Dementia Alzheimer's Type, Sensory Loss, Transient Ischaemic Attack
on Jan 21, 2005 Female patient from , 47 years of age, was diagnosed with progesterone decreased and was treated with Sarafem (View Usage). Patient had the following side effects: cerebrovascular accident, dementia alzheimer's type, sensory loss, transient ischaemic attack. Sarafem dosage: .


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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 Sarafem 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 Sarafem quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Sarafem 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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Sarafem Reactions
Anorexia
Apathy
ArrhythmiaWhat is Arrhythmia?
Asthenia
Blepharospasm
Bradycardia
Bronchopneumonia
Caesarean Section
Cardiac ArrestWhat is Cardiac arrest?
Cardio-respiratory Arrest
Cardiomegaly
Cerebrovascular Accident
ChokingWhat is Choking?
Corneal Abrasion
Crying
Cyanosis
Deafness
Dementia Alzheimer's Type
DepressionWhat is Depression?
Diarrhoea
DizzinessWhat is Dizziness?
Dry Eye
Dysgeusia
Dyspnoea
Feeling Abnormal
Hypotension
Hypoxia
Pharyngeal Oedema
Serotonin Syndrome
Throat Irritation
Sarafem 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 Sarafem 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!