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Summary

FDA Adverse Reports: 121. View All

Prometrium FDA safety alerts: No

Reported deaths: 3

Reported hospitalizations: 23

Prometrium Dosage, Warnings, Usage.

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

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Showing 1-50 of 121  Next Page  >

6878415-1 | Abortion Spontaneous, Vaginal Haemorrhage
on Oct 14, 2009 Female patient from UNITED STATES , 23 years of age, weighting 220.5 lb, was diagnosed with progesterone abnormal and was treated with Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: abortion spontaneous, vaginal haemorrhage. Prometrium dosage: 200 Milligram (s) Bid Oral Daily Dose: 400 Milligram (s). Patient was hospitalized.

6878414-X | Deep Vein Thrombosis, Off Label Use
Patient was taking Prometrium (View Usage). Patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?), off label use on Mar 03, 2010 from UNITED STATES Additional patient health information: Female patient , 47 years of age, was diagnosed with uterine leiomyoma, contraception, menorrhagia and. Prometrium dosage: Daily, Daily Dose. During the same period patient was treated with NUVARING (Daily, Daily Dose) (View Nuvaring Review and Nuvaring Label ). Patient was hospitalized.

6771154-7 | Depression, Dizziness, Dysarthria, Loss Of Consciousness, Nausea
Adverse event was reported on Jun 08, 2010 by a Female patient taking Prometrium (View Usage) (Dosage: Daily Dose: 400 Milligram(s)) was diagnosed with amenorrhoea and. Location: UNITED STATES , weighting 160.3 lb, After Prometrium was administered, patient had the following side effects: depression (What is depression?), dizziness (What is dizziness?), dysarthria, loss of consciousness, nausea (What is nausea?).

6722856-X | Dizziness, Headache, Hypoaesthesia Oral, Product Quality Issue
on May 12, 2010 Female patient from UNITED STATES , weighting 130.3 lb, was diagnosed with autonomic nervous system imbalance and was treated with Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), headache (What is headache?), hypoaesthesia oral, product quality issue. Prometrium dosage: 100mg=1cap Once Daily Po. During the same period patient was treated with VIVELLE DOT (View Vivelle-dot Review and Vivelle-dot Label ).


6680861-6 | Abasia, Gait Disturbance, Movement Disorder, Muscle Disorder, Muscle Injury, Muscle Spasms, Pain In Extremity, Weight Bearing Difficulty
on Apr 13, 2010 Female patient from UNITED STATES , 52 years of age, weighting 125.0 lb, was diagnosed with menopause (What is menopause?) and was treated with Prometrium (View Usage). Patient had the following side effects: abasia, gait disturbance, movement disorder (What is movement disorder?), muscle disorder (What is muscle disorder?), muscle injury, muscle spasms, pain in extremity, weight bearing difficulty. Prometrium dosage: 1 Capsule Once/day Po. During the same period patient was treated with ESTROGEN PATCH (View Estrogen Patch Review and Estrogen Patch Label ), VIVEL DOT (View Vivel Dot Review and Vivel Dot Label ).

6600815-5 | Fatigue, Headache, Rash, Vaginal Ulceration, Vulvovaginal Dryness
Patient was taking Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: fatigue, headache (What is headache?), rash (What is rash?), vaginal ulceration, vulvovaginal dryness on Feb 23, 2010 from UNITED STATES Additional patient health information: Female patient , 34 years of age, weighting 210.0 lb, was diagnosed with luteal phase deficiency and. Prometrium dosage: 200mg Daily Po.

6590111-7 | Depression, Suicidal Ideation
Adverse event was reported on Feb 13, 2009 by a Female patient taking Prometrium (View Usage) (Dosage: 100 Milligram(s) Qd Oral Daily Dose: 100 Milligram(s), 100 Milligram(s) Qd Oral Daily Dose: 100 Mill) . Location: UNITED STATES , 59 years of age, weighting 149.9 lb, Patient experienced the following unwanted or unexpected effects: depression (What is depression?), suicidal ideation. During the same period patient was treated with VIVELLE PATCH (ESTRADIOL) (View Vivelle Patch (estradiol) Review and Vivelle Patch (estradiol) Label ).

6589966-1 | Choking
on May 26, 2009 Female patient from UNITED STATES , 56 years of age, weighting 122.3 lb, was treated with Prometrium (View Usage). Patient had the following side effects: choking (What is choking?). Prometrium dosage: 100 Milligram(s) Qd Oral Daily Dose: 100 Milligram(s).

6568913-2 | Haemorrhage, Metrorrhagia
on Feb 01, 2010 Female patient from UNITED STATES , weighting 152.0 lb, was diagnosed with uterine leiomyoma and was treated with Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: haemorrhage, metrorrhagia. Prometrium dosage: 1 Pill Once Daily. During the same period patient was treated with DNA (View Dna Review and Dna Label ).

6558398-4 | Abasia, Dyspnoea, Euphoric Mood, Hypotonia, Inappropriate Affect, Pharyngeal Oedema
Patient was taking Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: abasia, dyspnoea, euphoric mood, hypotonia, inappropriate affect, pharyngeal oedema on Jan 28, 2010 from UNITED STATES Additional patient health information: Female patient , 39 years of age, weighting 150.0 lb, was diagnosed with menstruation irregular and. Prometrium dosage: 200 Mg 1 Capsule Each Day.

6535012-5 | Depression
Adverse event was reported on Jan 11, 2010 by a Female patient taking Prometrium (View Usage) (Dosage: ) was diagnosed with hot flush, menopausal symptoms and. Location: UNITED STATES , 59 years of age, weighting 115.0 lb, Patient had the following side effects: depression (What is depression?). During the same period patient was treated with VIVELLE DOT (View Vivelle-dot Review and Vivelle-dot Label ).

6439847-9 | Abasia, Aphasia, Eye Rolling, Hypotension
on Nov 12, 2009 Female patient from UNITED STATES , 49 years of age, weighting 140.0 lb, was diagnosed with hyperplasia and was treated with Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: abasia, aphasia (What is aphasia?), eye rolling, hypotension. Prometrium dosage: 200 Mg 1daily 12days.

6355998-1 | Balance Disorder, Confusional State, Dizziness, Dysarthria, Presyncope, Thinking Abnormal, Visual Impairment
on Sep 11, 2009 Female patient from UNITED STATES , weighting 129.2 lb, was diagnosed with menstrual disorder and was treated with Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: balance disorder, confusional state, dizziness (What is dizziness?), dysarthria, presyncope, thinking abnormal, visual impairment. Prometrium dosage: 200mg 1x Day Mouth. Patient was hospitalized.

6311672-9 | Antepartum Haemorrhage
Patient was taking Prometrium (View Usage). Patient had the following side effects: antepartum haemorrhage on Aug 03, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 140.0 lb, was diagnosed with prenatal care and. Prometrium dosage: Daily Dose: 100 Milligram(s).

6254151-X | Chest Discomfort, Hypoaesthesia
Adverse event was reported on Dec 01, 2008 by a Female patient taking Prometrium (View Usage) (Dosage: 400 Milligram(s) Qd Oral Daily Dose: 400 Milligram(s) Once) was diagnosed with ill-defined disorder and. Location: UNITED STATES , 66 years of age, weighting 112.4 lb, After Prometrium was administered, patient had the following side effects: chest discomfort, hypoaesthesia. Patient was hospitalized.

6254148-X | Abortion Spontaneous
on Sep 30, 2008 Female patient from UNITED STATES , 34 years of age, weighting 130.1 lb, was diagnosed with abortion (What is abortion?), prophylaxis and was treated with Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: abortion spontaneous. Prometrium dosage: 200 Milligram(s) Qd Oral Daily Dose: 200 Milligram(s). During the same period patient was treated with PRENATAL (View Prenatal Review and Prenatal Label ).

6254147-8 | Abortion Spontaneous
on Jul 30, 2008 Female patient from UNITED STATES , 32 years of age, weighting 124.6 lb, was diagnosed with prenatal care and was treated with Prometrium (View Usage). Patient had the following side effects: abortion spontaneous. Prometrium dosage: 400 Milligram(s) Qd Oral Daily Dose: 400 Milligram(s).

6254146-6 | Abdominal Pain, Abortion Spontaneous, Fatigue, Nausea
Patient was taking Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), abortion spontaneous, fatigue, nausea (What is nausea?) on Jun 09, 2008 from UNITED STATES Additional patient health information: Female patient , 28 years of age, weighting 124.6 lb, was diagnosed with progesterone decreased and. Prometrium dosage: 200 Milligram(s) Qd Oral Daily Dose: 200 Milligram(s).

6254135-1 | Abortion Spontaneous
Adverse event was reported on May 20, 2008 by a Female patient taking Prometrium (View Usage) (Dosage: 200 Milligram(s) Qd Oral Daily Dose: 200 Milligram(s)) was diagnosed with prenatal care and. Location: UNITED STATES , 34 years of age, weighting 180.8 lb, Patient experienced the following unwanted or unexpected effects: abortion spontaneous.

6208537-X | Pleural Effusion
on May 20, 2009 Female patient from UNITED STATES , weighting 170.4 lb, was diagnosed with menstruation irregular and was treated with Prometrium (View Usage). Patient had the following side effects: pleural effusion. Prometrium dosage: Daily Dose: 100 Milligram(s), As Used: 100 Mg, Frequency: 21 Days On 7 Days Off, Monthly.

6084997-2 | Lung Neoplasm Malignant, Oral Administration Complication
on Feb 13, 2009 Female patient from UNITED STATES , 84 years of age, was treated with Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: lung neoplasm malignant, oral administration complication. Prometrium dosage: .

6072891-2 | Cerebrovascular Accident
Patient was taking Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident on Jul 31, 2008 from UNITED STATES Additional patient health information: Female patient , 72 years of age, weighting 176.4 lb, was diagnosed with sleep disorder (What is sleep disorder?) and. Prometrium dosage: Daily Oral.

6072831-6 | Breast Cancer In Situ
Adverse event was reported on Jun 20, 2008 by a Female patient taking Prometrium (View Usage) (Dosage: Daily Oral) . Location: UNITED STATES , 47 years of age, Patient had the following side effects: breast cancer in situ. During the same period patient was treated with ESTRATAB (Daily Oral) (View Estratab Review and Estratab Label ), ESTRATEST (Daily Oral) (View Estratest Review and Estratest Label ), OGEN (Daily Oral) (View Ogen Review and Ogen Label ), PROVERA (Daily Oral) (View Provera Review and Provera Label ), PREMARIN (Daily Oral) (View Premarin Review and Premarin Label ), ORTHO PREFEST (ESTRADIOL/ESTRADIOL/NORGESTIMATE) (Daily Oral) (View Ortho-prefest (estradiol/estradiol/norgestimate) Review and Ortho-prefest (estradiol/estradiol/norgestimate) Label ), ACTIVELLA (Daily Oral) (View Activella Review and Activella Label ).

5918485-8 | Abdominal Pain Upper, Anxiety, Blood Pressure Increased, Chest Pain, Depressed Level Of Consciousness, Diarrhoea, Dyspepsia, Fatigue, Haemorrhagic Ovarian Cyst
on Oct 06, 2008 Female patient from UNITED STATES , weighting 149.9 lb, was diagnosed with ovarian cyst (What is ovarian cyst?), neck pain and was treated with Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: abdominal pain upper, anxiety (What is anxiety?), blood pressure increased, chest pain (What is chest pain?), depressed level of consciousness, diarrhoea, dyspepsia, fatigue, haemorrhagic ovarian cyst. Prometrium dosage: Daily Dose: 100 Milligram(s). During the same period patient was treated with YAZ (View Yaz Review and Yaz Label ), VICODIN (Daily Dose: 1 To 2 Tablets) (View Vicodin Review and Vicodin Label ), TYLENOL (CAPLET) (View Tylenol (caplet) Review and Tylenol (caplet) Label ), IBUPROFEN TABLETS (View Ibuprofen Tablets Review and Ibuprofen Tablets Label ). Patient was hospitalized.

5806996-5 | Pulmonary Embolism
on May 21, 2007 Female patient from UNITED STATES , 19 years of age, weighting 134.5 lb, was diagnosed with oligomenorrhoea and was treated with Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: pulmonary embolism (What is pulmonary embolism?). Prometrium dosage: Daily Oral Daily Dose: 100 Mg Daily For Days 1 Through 12 Of The Month. Patient was hospitalized.

5806993-X | Dizziness, Electrocardiogram Abnormal, Hemiparesis, Motor Dysfunction, Transient Ischaemic Attack
Patient was taking Prometrium (View Usage). Patient had the following side effects: dizziness (What is dizziness?), electrocardiogram abnormal, hemiparesis, motor dysfunction, transient ischaemic attack on Jun 29, 2007 from UNITED STATES Additional patient health information: Female patient , 43 years of age, weighting 178.6 lb, was diagnosed with uterine haemorrhage and. Prometrium dosage: Oral Daily Dose: 200 Mg Daily First Ten Days Of The Month. Patient was hospitalized.

5806987-4 | Abortion Spontaneous
Adverse event was reported on Apr 15, 2008 by a Female patient taking Prometrium (View Usage) (Dosage: 200 Milligram(s) Qd Oral Daily Dose: 200 Milligram(s)) was diagnosed with pregnancy (What is pregnancy?) and. Location: UNITED STATES , 22 years of age, weighting 156.5 lb, After Prometrium was administered, patient had the following side effects: abortion spontaneous.

5806968-0 | Abortion Spontaneous
on Dec 19, 2007 Female patient from UNITED STATES , 29 years of age, weighting 199.5 lb, was diagnosed with prenatal care, progesterone decreased and was treated with Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: abortion spontaneous. Prometrium dosage: 200 Milligram(s) Qd Oral Daily Dose: 200 Milligram(s). During the same period patient was treated with PRENATAL VITAMINS (PRENATAL VITAMINS) (View Prenatal Vitamins (prenatal Vitamins) Review and Prenatal Vitamins (prenatal Vitamins) Label ).

5806963-1 | Abortion Spontaneous, Dizziness, Nausea
on Nov 27, 2007 Female patient from UNITED STATES , 36 years of age, weighting 306.4 lb, was diagnosed with prenatal care, progesterone decreased and was treated with Prometrium (View Usage). Patient had the following side effects: abortion spontaneous, dizziness (What is dizziness?), nausea (What is nausea?). Prometrium dosage: 200 Milligram(s) Bid Oral Daily Dose: 400 Milligram(s). During the same period patient was treated with PRENATAL VITAMINS (PRENATAL VITAMINS) (View Prenatal Vitamins (prenatal Vitamins) Review and Prenatal Vitamins (prenatal Vitamins) Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ).

5806955-2 | Abortion Spontaneous
Patient was taking Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: abortion spontaneous on Nov 26, 2007 from UNITED STATES Additional patient health information: Female patient , 37 years of age, weighting 100.3 lb, was diagnosed with prenatal care and. Prometrium dosage: 100 Milligram(s) Qd Vaginal Daily Dose: 100 Milligram(s).

5806953-9 | Abortion Spontaneous
Adverse event was reported on Oct 30, 2007 by a Female patient taking Prometrium (View Usage) (Dosage: 200 Milligram(s) Bid Vaginal Daily Dose: 400 Milligram(s)) was diagnosed with prenatal care and. Location: UNITED STATES , 29 years of age, weighting 124.6 lb, Patient experienced the following unwanted or unexpected effects: abortion spontaneous. During the same period patient was treated with HUMALOG (View Humalog Review and Humalog Label ).

5806945-X | Abortion Spontaneous
on Oct 30, 2007 Female patient from UNITED STATES , 28 years of age, weighting 124.6 lb, was diagnosed with complication of pregnancy and was treated with Prometrium (View Usage). Patient had the following side effects: abortion spontaneous. Prometrium dosage: 200 Milligram(s) Bid Vaginal Daily Dose: 400 Milligram(s). During the same period patient was treated with HUMALOG (View Humalog Review and Humalog Label ).

5806917-5 | Deep Vein Thrombosis
on Oct 16, 2007 Female patient from UNITED STATES , 34 years of age, was diagnosed with in vitro fertilisation and was treated with Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?). Prometrium dosage: Daily Dose. During the same period patient was treated with FEMTRACE (Daily Oral Daily Dose) (View Femtrace Review and Femtrace Label ), GANIRELIX ACETATE INJECTION (Daily Subcutaneous Daily Dose) (View Ganirelix Acetate Injection Review and Ganirelix Acetate Injection Label ), FOLLISTIM (Daily Subcutaneous Daily Dose) (View Follistim Review and Follistim Label ), MENOPUR (Daily Subcutaneous Daily Dose) (View Menopur Review and Menopur Label ), CHORIOGONADOTROPIN (CHORIOGONADOTROPIN) (Daily Subcutaneous Daily Dose) (View Choriogonadotropin (choriogonadotropin) Review and Choriogonadotropin (choriogonadotropin) Label ), PROGESTERONE (Daily Subcutaneous Daily Dose) (View Progesterone Review and Progesterone Label ), PRENATAL VITAMINS (PRENATAL VITAMINS) (View Prenatal Vitamins (prenatal Vitamins) Review and Prenatal Vitamins (prenatal Vitamins) Label ). Patient was hospitalized.

5806844-3 | Breast Cancer
Patient was taking Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: breast cancer (What is breast cancer?) on Aug 27, 2007 from UNITED STATES Additional patient health information: Female patient , 32 years of age, . Prometrium dosage: Daily Oral Daily Dose. During the same period patient was treated with PREMARIN (Daily Dose) (View Premarin Review and Premarin Label ), MEDROXYPROGESTERONE (Daily Dose) (View Medroxyprogesterone Review and Medroxyprogesterone Label ), PREMPHASE (PREMARIN;CYCRIN 14/14) (Daily Dose) (View Premphase (premarin;cycrin 14/14) Review and Premphase (premarin;cycrin 14/14) Label ).

5806838-8 | Abdominal Pain Lower, Ovarian Cyst
Adverse event was reported on Aug 06, 2007 by a Female patient taking Prometrium (View Usage) (Dosage: Daily Dose) was diagnosed with infertility (What is infertility?) and. Location: UNITED STATES , 27 years of age, weighting 116.8 lb, Patient had the following side effects: abdominal pain lower, ovarian cyst (What is ovarian cyst?). During the same period patient was treated with CLOMID (100 Milligram(s) Qd Oral Daily Dose: 100 Milligram(s)) (View Clomid Review and Clomid Label ), ESTROGENIC SUBSTANCE (3 Milligram(s) Bid Oral Daily Dose: 6 Milligram(s)) (View Estrogenic Substance Review and Estrogenic Substance Label ), PRENATAL VITAMINS (PRENATAL VITAMINS) (View Prenatal Vitamins (prenatal Vitamins) Review and Prenatal Vitamins (prenatal Vitamins) Label ).

5806832-7 | Blighted Ovum, Blood Human Chorionic Gonadotropin Decreased, Dizziness, Progesterone Decreased
on Jun 14, 2007 Female patient from UNITED STATES , 28 years of age, weighting 160.9 lb, was diagnosed with prenatal care and was treated with Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: blighted ovum, blood human chorionic gonadotropin decreased, dizziness (What is dizziness?), progesterone decreased. Prometrium dosage: See Image.

5739779-5 | Apathy, Balance Disorder, Dizziness, Feeling Abnormal, Nausea, Somnolence
on May 12, 2008 Female patient from UNITED STATES , 38 years of age, weighting 240.0 lb, was diagnosed with menorrhagia and was treated with Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: apathy, balance disorder, dizziness (What is dizziness?), feeling abnormal, nausea (What is nausea?), somnolence. Prometrium dosage: 400 Mg 1x/day Po.

5703009-0 | Alopecia, Connective Tissue Disorder, Nasopharyngitis, Oedema Peripheral, Pain In Extremity
Patient was taking Prometrium (View Usage). Patient had the following side effects: alopecia, connective tissue disorder (What is connective tissue disorder?), nasopharyngitis, oedema peripheral, pain in extremity on Mar 25, 2008 from UNITED STATES Additional patient health information: Female patient , 59 years of age, weighting 191.8 lb, was diagnosed with connective tissue disorder (What is connective tissue disorder?) and. Prometrium dosage: 100 Mg;daily;oral. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PREDNISONE TAB (10 Mg;daily;oral : 10 Mg;daily;oral) (View Prednisone Tab Review and Prednisone Tab Label ), ESTRADIOL (2 Mg;daily;oral) (View Estradiol Review and Estradiol Label ).

5701701-5 | Arthralgia, Arthropathy, Breast Tenderness, Crying, Depression, Fatigue, Gait Disturbance, Myalgia
Adverse event was reported on Apr 09, 2008 by a Female patient taking Prometrium (View Usage) (Dosage: 100mg 1 Bedtime Po) was diagnosed with blood oestrogen abnormal and. Location: UNITED STATES , 54 years of age, weighting 185.0 lb, After Prometrium was administered, patient had the following side effects: arthralgia, arthropathy, breast tenderness, crying, depression (What is depression?), fatigue, gait disturbance, myalgia.

5688298-3 | Abortion Spontaneous
on Mar 19, 2008 Female patient from CANADA , 36 years of age, was treated with Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: abortion spontaneous. Prometrium dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ).

5670544-3 | Abortion Spontaneous
on Mar 05, 2008 Female patient from CANADA , 36 years of age, was treated with Prometrium (View Usage). Patient had the following side effects: abortion spontaneous. Prometrium dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ).

5670296-7 | Alopecia, Connective Tissue Disorder, Nasopharyngitis
Patient was taking Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: alopecia, connective tissue disorder (What is connective tissue disorder?), nasopharyngitis on Mar 07, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 191.8 lb, was diagnosed with connective tissue disorder (What is connective tissue disorder?) and. Prometrium dosage: Daily Dose: 100 Milligram(s). During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PREDNISONE TAB (Daily Dose: Medro Dose Pack) (View Prednisone Tab Review and Prednisone Tab Label ), ESTRADIOL (Daily Dose: 2 Milligram(s)) (View Estradiol Review and Estradiol Label ).

5662065-9 | Breast Cancer
Adverse event was reported on Dec 29, 2006 by a Female patient taking Prometrium (View Usage) (Dosage: Daily Oral) was diagnosed with menopausal symptoms and. Location: UNITED STATES , 74 years of age, Patient experienced the following unwanted or unexpected effects: breast cancer (What is breast cancer?). During the same period patient was treated with ESTRADIOL (View Estradiol Review and Estradiol Label ), ESTRACE (View Estrace Review and Estrace Label ).

5662063-5 | Breast Cancer
on Dec 19, 2006 Female patient from UNITED STATES , 59 years of age, was diagnosed with menopausal symptoms and was treated with Prometrium (View Usage). Patient had the following side effects: breast cancer (What is breast cancer?). Prometrium dosage: Daily Oral. During the same period patient was treated with ESTRACE (View Estrace Review and Estrace Label ), MEDROXYPROGESTERONE (View Medroxyprogesterone Review and Medroxyprogesterone Label ), PROVERA (Daily Oral) (View Provera Review and Provera Label ), ESTRADIOL (View Estradiol Review and Estradiol Label ).

5662061-1 | Breast Cancer
on Nov 12, 2007 Female patient from UNITED STATES , 64 years of age, was diagnosed with menopausal symptoms and was treated with Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: breast cancer (What is breast cancer?). Prometrium dosage: . During the same period patient was treated with ESTRATAB (View Estratab Review and Estratab Label ), PREMARIN (View Premarin Review and Premarin Label ), PROVERA (View Provera Review and Provera Label ), PREMPRO (View Prempro Review and Prempro Label ).

5662059-3 | Dyspnoea, Throat Tightness
Patient was taking Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, throat tightness on Mar 20, 2007 from UNITED STATES Additional patient health information: Female patient , weighting 141.1 lb, . Prometrium dosage: 200 Milligram(s) Qd Oral Daily Dose: 200 Milligram(s). During the same period patient was treated with ACTIVELLA (View Activella Review and Activella Label ).

5662043-X | Breast Cancer
Adverse event was reported on Mar 05, 2007 by a Female patient taking Prometrium (View Usage) (Dosage: ) . Location: UNITED STATES , 70 years of age, Patient had the following side effects: breast cancer (What is breast cancer?). During the same period patient was treated with PREMARIN (Daily Oral) (View Premarin Review and Premarin Label ), MEDROXYPROGESTERONE (View Medroxyprogesterone Review and Medroxyprogesterone Label ).

5662036-2 | Swollen Tongue, Thirst
on Feb 05, 2007 Female patient from UNITED STATES , weighting 140.0 lb, was treated with Prometrium (View Usage). After Prometrium was administered, patient had the following side effects: swollen tongue, thirst. Prometrium dosage: See Image. During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ).

5662034-9 | Abdominal Distension, Abdominal Pain, Amnesia, Anxiety, Dizziness, Fatigue, Irritability, Nausea, Suicidal Ideation
on Jan 05, 2007 Female patient from UNITED STATES , weighting 95.90 lb, was treated with Prometrium (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal distension, abdominal pain (What is abdominal pain?), amnesia, anxiety (What is anxiety?), dizziness (What is dizziness?), fatigue, irritability, nausea (What is nausea?), suicidal ideation. Prometrium dosage: 400 Milligram(s) Qd Oral Daily Dose: 400 Milligram(s). During the same period patient was treated with VIVELLE (View Vivelle Review and Vivelle Label ).

5601338-2 | Bronchial Neoplasm, Haemoptysis
Patient was taking Prometrium (View Usage). Patient had the following side effects: bronchial neoplasm, haemoptysis on Jan 14, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 139.3 lb, was diagnosed with menopausal symptoms and. Prometrium dosage: Daily Dose: 200 Milligram(s). During the same period patient was treated with PROGESTERONE (Daily Dose: 200 Milligram(s)) (View Progesterone Review and Progesterone Label ). Patient was hospitalized.

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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 Prometrium 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 Prometrium quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Prometrium 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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About Prometrium : Risks and Benefits, News and Updates, Prometrium video and TV resources

Prometrium 100 mg. Side Effect Report#2827 InsomniaFelt like a stimulate, achy and restless legs, absolutely could not sleep.

Prometrium Side Effects Report #SELF-4645 Female patient reported the following Prometrium side effect(s):dry mouth, and swollen tongue Event date: Friday December ...

Prometrium Side Effects - Complete Patient's Guide | User Reviews: Female patient, 23 years of age, weighting 220.5 |Weight|Feel Drunk. About Prometrium : Risks and ...

During the same period patient was treated with PROMETRIUM (Daily Dose: 1000 Milligram(s)) (View Prometrium Review and Prometrium Label ), FOLLICLE STIMULATING HORMONE ...

About Cyclogest : Risks and Benefits, News and Updates, Cyclogest video and TV resources

I took Clomid for the first week, along with Estrace and now on cycle day 12 (today) I was just prescribed Prometrium. I am reading online and it says this drug is to ...

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Estratest Side Effects - Complete Patient's Guide | User Reviews: Female patient, weighting 260.5 lb, was diagnosed with |Acne|Body Acne|Hair Loss|Pain In Hands And ...

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Prometrium Reactions
Abasia
Abdominal PainWhat is Abdominal pain?
Abnormal Behaviour
Abortion Spontaneous
Alopecia
Amnesia
AnxietyWhat is Anxiety?
Balance Disorder
Breast CancerWhat is Breast cancer?
Breast Cancer In Situ
Cerebrovascular Accident
Connective Tissue DisorderWhat is Connective tissue disorder?
Deep Vein ThrombosisWhat is Deep vein thrombosis?
DepressionWhat is Depression?
Diarrhoea
DizzinessWhat is Dizziness?
Dysarthria
Dyskinesia
Dyspnoea
DystoniaWhat is Dystonia?
Electrocardiogram Abnormal
Fatigue
Feeling Abnormal
Gait Disturbance
Loss Of Consciousness
NauseaWhat is Nausea?
Somnolence
Transient Ischaemic Attack
Urticaria
Vomiting
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