Please choose an event type to view the corresponding MedsFacts report:

HOT FLUSH ( 30 FDA reports)
METRORRHAGIA ( 28 FDA reports)
VAGINAL HAEMORRHAGE ( 24 FDA reports)
HEADACHE ( 20 FDA reports)
ALOPECIA ( 19 FDA reports)
SYNCOPE ( 19 FDA reports)
VERTIGO ( 17 FDA reports)
CHILLS ( 15 FDA reports)
HYPERHIDROSIS ( 15 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
ANXIETY ( 12 FDA reports)
FATIGUE ( 11 FDA reports)
NAUSEA ( 11 FDA reports)
PAIN IN EXTREMITY ( 11 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 11 FDA reports)
BREAST PAIN ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
NERVOUSNESS ( 9 FDA reports)
BREAST TENDERNESS ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
NO ADVERSE EVENT ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
ANEURYSM ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
BREAST SWELLING ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
PAIN ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
DEPRESSED MOOD ( 5 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
INJECTION SITE ERYTHEMA ( 5 FDA reports)
INJECTION SITE PRURITUS ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
VOMITING ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GENITAL HAEMORRHAGE ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
INJECTION SITE NODULE ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
LARYNGEAL OEDEMA ( 4 FDA reports)
LORDOSIS ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
MENORRHAGIA ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
RETINAL VEIN THROMBOSIS ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
LIBIDO DECREASED ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OSTEOCHONDROSIS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
UTERINE ENLARGEMENT ( 3 FDA reports)
UTERINE HAEMORRHAGE ( 3 FDA reports)
ACNE ( 2 FDA reports)
ADNEXA UTERI PAIN ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
BENIGN BREAST NEOPLASM ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD CORTICOTROPHIN INCREASED ( 2 FDA reports)
BLOOD CORTISOL INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD OESTROGEN DECREASED ( 2 FDA reports)
BREAST CANCER STAGE I ( 2 FDA reports)
BREAST ENLARGEMENT ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 2 FDA reports)
ENERGY INCREASED ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEMALE PATTERN BALDNESS ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PREMENSTRUAL SYNDROME ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROTHROMBIN TIME SHORTENED ( 2 FDA reports)
RASH ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 2 FDA reports)
SERUM FERRITIN ABNORMAL ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
URTICARIA LOCALISED ( 2 FDA reports)
VAGINAL INFECTION ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VULVOVAGINAL PRURITUS ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WITHDRAWAL BLEED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD OESTROGEN INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST INJURY ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG THERAPY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOMENORRHOEA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT INSTABILITY ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
OCULAR SURFACE DISEASE ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVARIAN DISORDER ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL TUBERCULOSIS ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBO-OVARIAN ABSCESS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VULVOVAGINAL DRYNESS ( 1 FDA reports)

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