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

DEPRESSION ( 27 FDA reports)
PAIN ( 27 FDA reports)
HEADACHE ( 23 FDA reports)
NAUSEA ( 23 FDA reports)
DRUG INEFFECTIVE ( 21 FDA reports)
DYSPNOEA ( 18 FDA reports)
PULMONARY EMBOLISM ( 18 FDA reports)
DIZZINESS ( 17 FDA reports)
UNINTENDED PREGNANCY ( 17 FDA reports)
CHOLECYSTITIS CHRONIC ( 16 FDA reports)
FATIGUE ( 16 FDA reports)
MYALGIA ( 16 FDA reports)
GALLBLADDER DISORDER ( 15 FDA reports)
VOMITING ( 15 FDA reports)
DEEP VEIN THROMBOSIS ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
ANXIETY ( 13 FDA reports)
CROHN'S DISEASE ( 13 FDA reports)
MENORRHAGIA ( 13 FDA reports)
RENAL FAILURE ACUTE ( 13 FDA reports)
DIARRHOEA ( 12 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 12 FDA reports)
LOSS OF CONSCIOUSNESS ( 12 FDA reports)
RASH ( 12 FDA reports)
BREAST CANCER ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
GENERALISED ANXIETY DISORDER ( 11 FDA reports)
MALIGNANT MELANOMA ( 11 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
PYELONEPHRITIS ( 11 FDA reports)
UVEITIS ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
CHOLELITHIASIS ( 10 FDA reports)
ARTHRALGIA ( 9 FDA reports)
ASTHMA ( 9 FDA reports)
BLOOD PRESSURE INCREASED ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
HYPOTENSION ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
NEPHRITIS INTERSTITIAL ( 8 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
AMENORRHOEA ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
EMOTIONAL DISTRESS ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
VAGINAL HAEMORRHAGE ( 7 FDA reports)
VERTIGO ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
CHOLECYSTECTOMY ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
DEATH ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
FALL ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
INJURY ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
MOOD SWINGS ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PANCREATITIS ( 6 FDA reports)
PREMATURE DELIVERY ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
ABORTION THREATENED ( 5 FDA reports)
AGITATION ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BONE DISORDER ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
COMPRESSION FRACTURE ( 5 FDA reports)
COUGH ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FEMORAL NECK FRACTURE ( 5 FDA reports)
FOOT FRACTURE ( 5 FDA reports)
GRAND MAL CONVULSION ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
JAUNDICE NEONATAL ( 5 FDA reports)
METRORRHAGIA ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
OSTEOMALACIA ( 5 FDA reports)
OSTEOPENIA ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
PELVIC FRACTURE ( 5 FDA reports)
PREGNANCY ( 5 FDA reports)
PREMATURE BABY ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
TREMOR ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
AGGRESSION ( 4 FDA reports)
BLOODY DISCHARGE ( 4 FDA reports)
BREAST CANCER FEMALE ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CRYING ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
MENOMETRORRHAGIA ( 4 FDA reports)
MUSCLE TWITCHING ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PLACENTAL DISORDER ( 4 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RASH SCARLATINIFORM ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SMALL FOR DATES BABY ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
UTERINE LEIOMYOMA ( 4 FDA reports)
VULVAL DISORDER ( 4 FDA reports)
ABORTION ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ANGER ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EPHELIDES ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FISTULA DISCHARGE ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
IUCD COMPLICATION ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MELANOCYTIC NAEVUS ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NO ADVERSE EFFECT ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 3 FDA reports)
PROCEDURAL PAIN ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RECTAL CANCER ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
STRESS ( 3 FDA reports)
THIRST ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 3 FDA reports)
VULVOVAGINAL DISCOMFORT ( 3 FDA reports)
VULVOVAGINAL PAIN ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANOVULATORY CYCLE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BREAST DYSPLASIA ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CYST ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATIC VEIN THROMBOSIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENSTRUAL DISORDER ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPORTS INJURY ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
UTERINE RUPTURE ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BARTHOLIN'S CYST ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL ENDOCRINE ANOMALY ( 1 FDA reports)
CONGENITAL TORTICOLLIS ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EARLY SATIETY ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ENDOMETRIAL HYPOPLASIA ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRODUODENITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC ADENOMA ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTELLIGENCE TEST ABNORMAL ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY LEVEL ABNORMAL ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE INFLAMMATION ( 1 FDA reports)
SPECIAL SENSES CONGENITAL ANOMALY ( 1 FDA reports)
SPONDYLOARTHROPATHY ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SUSAC'S SYNDROME ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UTERINE PERFORATION ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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